| Year |
Citation |
Score |
| 2023 |
Chambers KJ, Sanghong P, Carter Martos D, Casoni G, Mykura RC, Prasad Hari D, Noble A, Aggarwal VK. Stereospecific Conversion of Boronic Esters into Enones using Methoxyallene: Application in the Total Synthesis of 10-Deoxymethynolide. Angewandte Chemie (International Ed. in English). e202312054. PMID 37877778 DOI: 10.1002/anie.202312054 |
0.453 |
|
| 2023 |
Prévost S, Thai K, Schützenmeister N, Coulthard G, Erb W, Aggarwal VK. Correction to "Synthesis of Prostaglandin Analogues, Latanoprost and Bimatoprost, Using Organocatalysis via a Key Bicyclic Enal Intermediate". Organic Letters. 25: 6235. PMID 37566563 DOI: 10.1021/acs.orglett.3c02579 |
0.375 |
|
| 2023 |
Pagire SK, Shu C, Reich D, Noble A, Aggarwal VK. Convergent Deboronative and Decarboxylative Phosphonylation Enabled by the Phosphite Radical Trap "BecaP". Journal of the American Chemical Society. 145: 18649-18657. PMID 37552886 DOI: 10.1021/jacs.3c06524 |
0.799 |
|
| 2023 |
Wu J, Shu C, Li Z, Noble A, Aggarwal VK. Photoredox-Catalyzed Decarboxylative Bromination, Chlorination and Thiocyanation Using Inorganic Salts. Angewandte Chemie (International Ed. in English). e202309684. PMID 37522816 DOI: 10.1002/anie.202309684 |
0.429 |
|
| 2023 |
Shen HC, Popescu MV, Wang ZS, de Lescure L, Noble A, Paton RS, Aggarwal VK. Iridium-Catalyzed Asymmetric Difunctionalization of C-C σ-Bonds Enabled by Ring-Strained Boronate Complexes. Journal of the American Chemical Society. PMID 37471704 DOI: 10.1021/jacs.3c03248 |
0.345 |
|
| 2023 |
Wang ZS, Bennett SH, Kicin B, Jing C, Pradeilles JA, Thai K, Smith JR, Bacoş PD, Fasano V, Saunders CM, Aggarwal VK. De Novo Synthesis of Dihydrobenzofurans and Indolines and Its Application to a Modular, Asymmetric Synthesis of Beraprost. Journal of the American Chemical Society. 145: 14124-14132. PMID 37326516 DOI: 10.1021/jacs.3c04582 |
0.453 |
|
| 2023 |
Bashir M, Arshad M, Begum R, Aggarwal VK. Application of Enantioselective Sulfur Ylide Epoxidation to a Short Asymmetric Synthesis of Bedaquiline, a Potent Anti-Tuberculosis Drug. Organic Letters. 25: 4281-4285. PMID 37284829 DOI: 10.1021/acs.orglett.3c01286 |
0.382 |
|
| 2023 |
Tyler J, Aggarwal VK. Synthesis and Applications of Bicyclo[1.1.0]butyl and Azabicyclo[1.1.0]butyl Organometallics. Chemistry (Weinheim An Der Bergstrasse, Germany). e202300008. PMID 36786481 DOI: 10.1002/chem.202300008 |
0.305 |
|
| 2023 |
Abell JC, Bold CP, Vicens L, Jentsch T, Velasco N, Tyler JL, Straker RN, Noble A, Aggarwal VK. Synthesis of Dihydropyridine Spirocycles by Semi-Pinacol-Driven Dearomatization of Pyridines. Organic Letters. 25: 400-404. PMID 36626565 DOI: 10.1021/acs.orglett.2c04095 |
0.358 |
|
| 2022 |
Wölfl B, Winter N, Li J, Noble A, Aggarwal VK. Strain-Release Driven Epoxidation and Aziridination of Bicyclo[1.1.0]butanes via Palladium Catalyzed σ-Bond Nucleopalladation. Angewandte Chemie (International Ed. in English). e202217064. PMID 36507714 DOI: 10.1002/anie.202217064 |
0.439 |
|
| 2022 |
Aiken SG, Bateman JM, Liao HH, Fawcett A, Bootwicha T, Vincetti P, Myers EL, Noble A, Aggarwal VK. Iterative synthesis of 1,3-polyboronic esters with high stereocontrol and application to the synthesis of bahamaolide A. Nature Chemistry. PMID 36424454 DOI: 10.1038/s41557-022-01087-9 |
0.435 |
|
| 2022 |
Tyler JL, Noble A, Aggarwal VK. Four-Component Strain-Release-Driven Synthesis of Functionalized Azetidines. Angewandte Chemie (International Ed. in English). e202214049. PMID 36300572 DOI: 10.1002/anie.202214049 |
0.313 |
|
| 2022 |
Wang H, Han W, Noble A, Aggarwal VK. Dual Nickel/Photoredox-Catalyzed Site-Selective Cross-Coupling of 1,2-Bis-Boronic Esters Enabled by 1,2-Boron Shifts. Angewandte Chemie (International Ed. in English). PMID 35779000 DOI: 10.1002/anie.202207988 |
0.406 |
|
| 2022 |
Fairchild ME, Noble A, Aggarwal VK. Diastereodivergent Synthesis of Cyclopentyl Boronic Esters Bearing Contiguous Fully Substituted Stereocenters. Angewandte Chemie (International Ed. in English). e202205816. PMID 35639345 DOI: 10.1002/anie.202205816 |
0.482 |
|
| 2022 |
Fiorito D, Keskin S, Bateman JM, George M, Noble A, Aggarwal VK. Stereocontrolled Total Synthesis of Bastimolide B Using Iterative Homologation of Boronic Esters. Journal of the American Chemical Society. PMID 35499478 DOI: 10.1021/jacs.2c03192 |
0.351 |
|
| 2022 |
Wang H, Wu J, Noble A, Aggarwal VK. Selective Coupling of 1,2-Bis-Boronic Esters at the more. Angewandte Chemie (International Ed. in English). PMID 35213775 DOI: 10.1002/anie.202202061 |
0.381 |
|
| 2021 |
Deeprose MJ, Lowe M, Noble A, Booker-Milburn KI, Aggarwal VK. Sequential Photocatalytic Reactions for the Diastereoselective Synthesis of Cyclobutane Scaffolds. Organic Letters. PMID 34882426 DOI: 10.1021/acs.orglett.1c03746 |
0.419 |
|
| 2021 |
Lewis-Borrell L, Sneha M, Clark IP, Fasano V, Noble A, Aggarwal VK, Orr-Ewing AJ. Direct Observation of Reactive Intermediates by Time-Resolved Spectroscopy Unravels the Mechanism of a Radical-Induced 1,2-Metalate Rearrangement. Journal of the American Chemical Society. PMID 34614354 DOI: 10.1021/jacs.1c07964 |
0.327 |
|
| 2021 |
Sang R, Noble A, Aggarwal VK. Chiral Benzothiophene Synthesis via Enantiospecific Coupling of Benzothiophene S-Oxides with Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 34582085 DOI: 10.1002/anie.202112180 |
0.369 |
|
| 2021 |
Fasano V, McFord AW, Butts CP, Collins BSL, Fey N, Alder RW, Aggarwal VK. Corrigendum: How Big is the Pinacol Boronic Ester as a Substituent? Angewandte Chemie (International Ed. in English). 60: 20087. PMID 34459082 DOI: 10.1002/anie.202106534 |
0.387 |
|
| 2021 |
Aggarwal VK, Humphries PS, Fenwick A. A Formal Asymmetric Synthesis of (+)-Anatoxin-a Using an Enantioselective Deprotonation Strategy on an Eight-Membered Ring. Angewandte Chemie (International Ed. in English). 38: 1985-1986. PMID 34182674 DOI: 10.1002/(SICI)1521-3773(19990712)38:13/14<1985::AID-ANIE1985>3.0.CO;2-7 |
0.445 |
|
| 2021 |
Hari DP, Madhavachary R, Fasano V, Haire J, Aggarwal VK. Highly Diastereoselective Strain-Increase Allylborations: Rapid Access to Alkylidenecyclopropanes and Alkylidenecyclobutanes. Journal of the American Chemical Society. PMID 33950678 DOI: 10.1021/jacs.1c01966 |
0.795 |
|
| 2021 |
White DH, Noble A, Booker-Milburn KI, Aggarwal VK. Diastereoselective Photoredox-Catalyzed [3 + 2] Cycloadditions of -Sulfonyl Cyclopropylamines with Electron-Deficient Olefins. Organic Letters. PMID 33821661 DOI: 10.1021/acs.orglett.1c00711 |
0.343 |
|
| 2021 |
Aggarwal VK, Tyler J, Noble A. Strain-Release Driven Spirocyclization of Azabicyclo[1.1.0]butyl Ketones. Angewandte Chemie (International Ed. in English). PMID 33754432 DOI: 10.1002/anie.202102754 |
0.332 |
|
| 2021 |
Aggarwal VK, Songara P, Luc E, Rogers J, Stammers E, Mykura R. Studies on the lithiation, borylation, and 1,2-metalate rearrangement of O-cycloalkyl 2,4,6-triisopropylbenzoates. Angewandte Chemie (International Ed. in English). PMID 33651488 DOI: 10.1002/anie.202101374 |
0.366 |
|
| 2020 |
Aggarwal VK, Guo L, Noble A. α-Selective Ring-Opening Reactions of Bicyclo[1.1.0]butyl Boronic Ester with Nucleophiles. Angewandte Chemie (International Ed. in English). PMID 32956541 DOI: 10.1002/Anie.202011739 |
0.461 |
|
| 2020 |
Aggarwal VK, Armstrong SK, Caggiano L, Chibale K, Clayden J, Coldham I, Greeves N, Hartley RC, Knight JG, Kuhnert N, Mitchell HJ, Nelson A, O'Brien P, Thomas SP, Wyatt P. Stuart Warren (24 Dec 1938-22 Mar 2020). Organic & Biomolecular Chemistry. PMID 32936190 DOI: 10.1039/D0Ob90121K |
0.736 |
|
| 2020 |
Shu C, Madhavachary R, Noble A, Aggarwal VK. Photoinduced Fragmentation Borylation of Cyclic Alcohols and Hemiacetals. Organic Letters. PMID 32903015 DOI: 10.1021/Acs.Orglett.0C02513 |
0.783 |
|
| 2020 |
Aggarwal VK, Lerchen A, Gandhamsetty N, Farrar E, Winter N, Platzek J, Grayson M. Enantioselective Total Synthesis of (-)-Finerenone using Asymmetric Transfer Hydrogenation. Angewandte Chemie (International Ed. in English). PMID 32890415 DOI: 10.1002/Anie.202011256 |
0.412 |
|
| 2020 |
Bennett S, Fawcett A, Denton E, Biberger T, Fasano V, Winter N, Aggarwal VK. Difunctionalization of C-C σ Bonds Enabled by the Reaction of Bicyclo[1.1.0]butyl Boronate Complexes with Electrophiles: Reaction Development, Scope, and Stereochemical Origins. Journal of the American Chemical Society. PMID 32885974 DOI: 10.1021/Jacs.0C07357 |
0.42 |
|
| 2020 |
Aggarwal VK, Fasano V, McFord AW, Butts CP, Collins BSL, Fey N, Alder RW. How big is the pinacol boronic ester as a substituent? Angewandte Chemie (International Ed. in English). PMID 32866342 DOI: 10.1002/Anie.202007776 |
0.402 |
|
| 2020 |
Jing C, Aggarwal VK. Total Synthesis of Thromboxane B via a Key Bicyclic Enal Intermediate. Organic Letters. 22: 6505-6509. PMID 32806168 DOI: 10.1021/Acs.Orglett.0C02299 |
0.496 |
|
| 2020 |
Bennett SH, Coulthard G, Aggarwal VK. Prostaglandin Total Synthesis Enabled by the Organocatalytic Dimerization of Succinaldehyde. Chemical Record (New York, N.Y.). PMID 32672398 DOI: 10.1002/Tcr.202000054 |
0.423 |
|
| 2020 |
Yu S, Jing C, Noble A, Aggarwal VK. Iridium-Catalyzed Enantioselective Synthesis of α-Chiral Bicyclo[1.1.1]pentanes by 1,3-Difunctionalization of [1.1.1]Propellane. Organic Letters. PMID 32638587 DOI: 10.1021/Acs.Orglett.0C02017 |
0.804 |
|
| 2020 |
Aggarwal VK, Wang H, Jing C, Noble A. Stereospecific 1,2-Migrations of Boronate Complexes Induced by Electrophiles. Angewandte Chemie (International Ed. in English). PMID 32592274 DOI: 10.1002/Anie.202008096 |
0.467 |
|
| 2020 |
Hari DP, Abell JC, Fasano V, Aggarwal VK. Ring-Expansion Induced 1,2-Metalate Rearrangements: Highly Diastereoselective Synthesis of Cyclobutyl Boronic Esters. Journal of the American Chemical Society. PMID 32146807 DOI: 10.1021/Jacs.0C00813 |
0.506 |
|
| 2020 |
Aggarwal VK, Fasano V, Winter N, Noble A. Divergent, stereospecific mono- and difluoromethylation of boronic esters. Angewandte Chemie (International Ed. in English). PMID 32109329 DOI: 10.1002/Anie.202002246 |
0.454 |
|
| 2020 |
Davenport R, Silvi M, Noble A, Hosni Z, Fey N, Aggarwal VK. Visible Light-Driven Strain-Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 31912963 DOI: 10.1002/Anie.201915409 |
0.796 |
|
| 2020 |
Yu S, Jing C, Noble A, Aggarwal VK. 1,3-Difunctionalizations of [1.1.1]Propellane via 1,2-Metallate Rearrangements of Boronate Complexes. Angewandte Chemie (International Ed. in English). PMID 31912941 DOI: 10.1002/Anie.201914875 |
0.783 |
|
| 2020 |
Mega RS, Duong VK, Noble A, Aggarwal VK. Decarboxylative Conjunctive Cross-coupling of Vinyl Boronic Esters using Metallaphotoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 31909870 DOI: 10.1002/Anie.201916340 |
0.491 |
|
| 2020 |
Aggarwal VK. The Bristol Synthesis Meeting – Fostering Creativity and Inspiration since 2001 European Journal of Organic Chemistry. 2020: 2308-2309. DOI: 10.1002/Ejoc.202000458 |
0.407 |
|
| 2020 |
Davenport R, Silvi M, Noble A, Hosni Z, Fey N, Aggarwal VK. Back Cover: Visible‐Light‐Driven Strain‐Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters (Angew. Chem. Int. Ed. 16/2020) Angewandte Chemie International Edition. 59: 6632-6632. DOI: 10.1002/Anie.202003607 |
0.797 |
|
| 2020 |
Davenport R, Silvi M, Noble A, Hosni Z, Fey N, Aggarwal VK. Rücktitelbild: Visible‐Light‐Driven Strain‐Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters (Angew. Chem. 16/2020) Angewandte Chemie. 132: 6694-6694. DOI: 10.1002/Ange.202003607 |
0.801 |
|
| 2019 |
Yu S, Noble A, Bedford RB, Aggarwal VK. Methylenespiro[2.3]hexanes via Nickel-Catalyzed Cyclopropanations with [1.1.1]Propellane. Journal of the American Chemical Society. PMID 31786925 DOI: 10.1021/Jacs.9B10689 |
0.792 |
|
| 2019 |
Nandakumar M, Rubial B, Noble A, Myer E, Aggarwal VK. Ring-Opening Lithiation-Borylation of 2-Trifluoromethyl Oxirane: A Route to Versatile Tertiary Trifluoromethyl Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 31710748 DOI: 10.1002/Anie.201912797 |
0.503 |
|
| 2019 |
Wu J, Baer R, Guo L, Noble A, Aggarwal VK. Photoinduced Deoxygenative Borylations of Aliphatic Alcohols. Angewandte Chemie (International Ed. in English). PMID 31613033 DOI: 10.1002/Anie.201910051 |
0.328 |
|
| 2019 |
Kaiser D, Noble A, Fasano V, Aggarwal VK. 1,2-Boron Shifts of β-Boryl Radicals Generated from Bis-Boronic Esters using Photoredox Catalysis. Journal of the American Chemical Society. PMID 31461622 DOI: 10.1021/Jacs.9B07564 |
0.479 |
|
| 2019 |
Aggarwal VK, Fordham JM, Grayson MN. Vinylidene Homologation of Boronic Esters and its Application to the Synthesis of the Proposed Structure of Machillene. Angewandte Chemie (International Ed. in English). PMID 31365776 DOI: 10.1002/Anie.201907617 |
0.5 |
|
| 2019 |
Silvi M, Aggarwal VK. Radical Addition to Strained σ-Bonds Enables the Stereocontrolled Synthesis of Cyclobutyl Boronic Esters. Journal of the American Chemical Society. PMID 31142107 DOI: 10.1021/Jacs.9B03653 |
0.795 |
|
| 2019 |
Gregson CHU, Ganesh V, Aggarwal VK. Strain Release of Donor-Acceptor Cyclopropyl Boronate Complexes. Organic Letters. PMID 31017445 DOI: 10.1021/Acs.Orglett.9B01152 |
0.79 |
|
| 2019 |
Fawcett A, Murtaza A, Gregson CHU, Aggarwal VK. Strain-Release-Driven Homologation of Boronic Esters: Application to the Modular Synthesis of Azetidines. Journal of the American Chemical Society. PMID 30836746 DOI: 10.1021/Jacs.9B01513 |
0.498 |
|
| 2019 |
Wu J, Grant PS, Li X, Noble A, Aggarwal VK. Catalyst-Free Deaminative Functionalizations of Primary Amines via Photoinduced Single-Electron Transfer. Angewandte Chemie (International Ed. in English). PMID 30794331 DOI: 10.1002/Anie.201814452 |
0.385 |
|
| 2019 |
Shu C, Noble A, Aggarwal VK. Photoredox-Catalyzed Cyclobutane Synthesis via a Deboronative Radical Addition-Polar Cyclization Cascade. Angewandte Chemie (International Ed. in English). PMID 30681266 DOI: 10.1002/Anie.201813917 |
0.508 |
|
| 2019 |
Fawcett A, Biberger T, Aggarwal VK. Carbopalladation of C-C σ-bonds enabled by strained boronate complexes. Nature Chemistry. 11: 117-122. PMID 30532013 DOI: 10.1038/S41557-018-0181-X |
0.444 |
|
| 2019 |
Li AH, Dai LX, Aggarwal VK. Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement. Chemical Reviews. 97: 2341-2372. PMID 11848902 DOI: 10.1021/Cr960411R |
0.482 |
|
| 2019 |
Aggarwal VK, Esquivel-Zamora BN, Evans GR, Jones E. Studies on the Asymmetric Oxidation of Ester Derivatives of 1,3-Dithiane-2-carboxylates. Asymmetric Synthesis of trans-1,3-Dithiane 1,3-Dioxide. The Journal of Organic Chemistry. 63: 7306-7310. PMID 11672376 DOI: 10.1021/Jo9807971 |
0.456 |
|
| 2019 |
Aggarwal VK, Mereu A, Tarver GJ, McCague R. Metal- and Ligand-Accelerated Catalysis of the Baylis-Hillman Reaction. The Journal of Organic Chemistry. 63: 7183-7189. PMID 11672359 DOI: 10.1021/Jo980421N |
0.422 |
|
| 2019 |
Bateman JM, Aggarwal VK. 1,2‐Metallate Rearrangement of Boron Derivatives Patai's Chemistry of Functional Groups. 1-96. DOI: 10.1002/9780470682531.Pat0973 |
0.394 |
|
| 2018 |
Rubial B, Collins BSL, Bigler R, Aichhorn S, Noble A, Aggarwal VK. Enantiospecific Synthesis of ortho-Substituted 1,1-Diarylalkanes by a 1,2-Metalate Rearrangement/anti-SN2' Elimination/Rearomatizing Allylic Suzuki-Miyaura Reaction Sequence. Angewandte Chemie (International Ed. in English). PMID 30520228 DOI: 10.1002/Anie.201811343 |
0.51 |
|
| 2018 |
Mykura RC, Veth S, Varela A, Dewis L, Farndon JJ, Myers EL, Aggarwal VK. Investigation of the Deprotonative Generation and Borylation of Diamine-Ligated α-Lithiated Carbamates and Benzoates by in situ IR spectroscopy. Journal of the American Chemical Society. PMID 30260635 DOI: 10.1021/Jacs.8B06871 |
0.421 |
|
| 2018 |
Ganesh V, Noble A, Aggarwal VK. Chiral Aniline Synthesis via Stereospecific C(sp)-C(sp) Coupling of Boronic Esters with Aryl Hydrazines. Organic Letters. PMID 30221524 DOI: 10.1021/Acs.Orglett.8B02615 |
0.799 |
|
| 2018 |
Shu C, Mega RS, Andreassen BJ, Noble A, Aggarwal VK. Synthesis of Functionalized Cyclopropanes from Carboxylic Acids via a Radical Addition-Polar Cyclization Cascade. Angewandte Chemie (International Ed. in English). PMID 30204292 DOI: 10.1002/Anie.201808598 |
0.463 |
|
| 2018 |
Wu J, He L, Noble A, Aggarwal VK. Photoinduced Deaminative Borylation of Alkylamines. Journal of the American Chemical Society. PMID 30091912 DOI: 10.1021/Jacs.8B07103 |
0.427 |
|
| 2018 |
Niwetmarin W, Rego Campello H, Sparkes HA, Aggarwal VK, Gallagher T. (-)-Cytisine: Access to a stereochemically defined and functionally flexible piperidine scaffold. Organic & Biomolecular Chemistry. PMID 30067256 DOI: 10.1039/C8Ob01456F |
0.335 |
|
| 2018 |
Pelss A, Gandhamsetty N, Smith JR, Mailhol D, Silvi M, Watson A, Perez-Powell I, Prévost S, Schützenmeister N, Moore P, Aggarwal VK. Re-optimization of the Organocatalyzed Double Aldol Domino Process to a Key Enal Intermediate and its Application to the Total Synthesis of Δ¹²-Prostaglandin J₃. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29774967 DOI: 10.1002/Chem.201802498 |
0.814 |
|
| 2018 |
Zhurakovskyi O, Dias RMP, Noble A, Aggarwal VK. Stereo- and Regiocontrolled Methylboration of Terminal Alkynes. Organic Letters. PMID 29741904 DOI: 10.1021/Acs.Orglett.8B01252 |
0.51 |
|
| 2018 |
Armstrong RJ, Nandakumar M, Dias RMP, Noble A, Myers EL, Aggarwal VK. Enantiodivergent Synthesis of Allenes by Point to Axial Chirality Transfer. Angewandte Chemie (International Ed. in English). PMID 29719111 DOI: 10.1002/Anie.201804446 |
0.512 |
|
| 2018 |
Silvi M, Schrof R, Noble A, Aggarwal VK. Enantiospecific Three-Component Alkylation of Furan and Indole. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29411914 DOI: 10.1002/Chem.201800527 |
0.803 |
|
| 2018 |
Noble A, Mega RS, Pflästerer D, Myers EL, Aggarwal VK. Visible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ-Amino Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 29316095 DOI: 10.1002/Anie.201712186 |
0.489 |
|
| 2018 |
Tillin C, Bigler R, Calo-Lapido R, Collins B, Noble A, Aggarwal V. Complex Boron-Containing Molecules through a 1,2-Metalate Rearrangement/anti-S
N
2′ Elimination/Cycloaddition Reaction Sequence Synlett. 30: 449-453. DOI: 10.1055/S-0037-1610389 |
0.462 |
|
| 2018 |
McGarrigle E, Aggarwal V, Fearraigh M, Matlock J, Illa O. Synthesis of Isothiocineole and Application in Multigram-Scale Sulfur Ylide Mediated Asymmetric Epoxidation and Aziridination Synthesis. 50: 3337-3343. DOI: 10.1055/S-0037-1609580 |
0.411 |
|
| 2017 |
Zhurakovskyi O, Türkmen YE, Löffler LE, Moorthie VA, Chen CC, Shaw MA, Crimmin MR, Ferrara M, Ahmad M, Ostovar M, Matlock JV, Aggarwal VK. Enantioselective Synthesis of the Cyclopiazonic Acid Family Using Sulfur Ylides. Angewandte Chemie (International Ed. in English). PMID 29265694 DOI: 10.1002/Anie.201712065 |
0.827 |
|
| 2017 |
Bigler R, Aggarwal VK. ortho-Directing Chromium Arene Complexes as Efficient Mediators for Enantiospecific C(sp2 )-C(sp3 ) Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). PMID 29227017 DOI: 10.1002/Anie.201711816 |
0.459 |
|
| 2017 |
Nakamura E, Winkler JD, Aggarwal VK. Gilbert Stork (1921-2017). Angewandte Chemie (International Ed. in English). PMID 29193592 DOI: 10.1002/Anie.201711474 |
0.679 |
|
| 2017 |
Millán A, Grigol Martínez P, Aggarwal VK. Stereocontrolled synthesis of polypropionate fragments based on a building block assembly strategy using lithiation-borylation methodologies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29156080 DOI: 10.1002/Chem.201704946 |
0.788 |
|
| 2017 |
Lorenzo P, Butts CP, Myers EL, Aggarwal VK. The Story behind "Synergy of Synthesis, Computation, and NMR Reveals Correct Baulamycin Structures". Biochemistry. PMID 29125284 DOI: 10.1021/Acs.Biochem.7B00994 |
0.311 |
|
| 2017 |
Wilson CM, Ganesh V, Noble A, Aggarwal VK. Enantiospecific sp²-sp³ Coupling of o- and p-Phenols with Secondary and Tertiary Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 29111609 DOI: 10.1002/Anie.201710777 |
0.761 |
|
| 2017 |
Baars H, Classen MJ, Aggarwal VK. Synthesis of Alfaprostol and PGF2α through 1,4-Addition of an Alkyne to an Enal Intermediate as the Key Step. Organic Letters. PMID 29064717 DOI: 10.1021/Acs.Orglett.7B03057 |
0.517 |
|
| 2017 |
García-Ruiz C, Chen JL, Sandford C, Feeney K, Lorenzo P, Berionni G, Mayr H, Aggarwal VK. Stereospecific Allylic Functionalization: The Reactivity of Allylboronate Complexes with Electrophiles. Journal of the American Chemical Society. PMID 29028321 DOI: 10.1021/Jacs.7B10240 |
0.453 |
|
| 2017 |
Bootwicha T, Feilner JM, Myers EL, Aggarwal VK. Iterative assembly line synthesis of polypropionates with full stereocontrol. Nature Chemistry. 9: 896-902. PMID 28837173 DOI: 10.1038/Nchem.2757 |
0.425 |
|
| 2017 |
Casoni G, Kucukdisli M, Fordham JM, Burns M, Myers EL, Aggarwal VK. α-Sulfinyl Benzoates as Precursors to Li and Mg Carbenoids for the Stereoselective Iterative Homologation of Boronic Esters. Journal of the American Chemical Society. PMID 28812893 DOI: 10.1021/Jacs.7B05457 |
0.449 |
|
| 2017 |
Pulis AP, Varela A, Citti C, Songara P, Leonori D, Aggarwal VK. Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α-Oxy- and α-Thio-Substituted Organolithium Species. Angewandte Chemie (International Ed. in English). PMID 28783238 DOI: 10.1002/Anie.201706722 |
0.676 |
|
| 2017 |
Wu J, Lorenzo P, Zhong S, Ali M, Butts CP, Myers EL, Aggarwal VK. Synergy of synthesis, computation and NMR reveals correct baulamycin structures. Nature. 547: 436-440. PMID 28748934 DOI: 10.1038/Nature23265 |
0.308 |
|
| 2017 |
Smith JR, Collins BSL, Hesse MJ, Graham MA, Myers EL, Aggarwal VK. Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes. Journal of the American Chemical Society. PMID 28665124 DOI: 10.1021/Jacs.7B05149 |
0.445 |
|
| 2017 |
Aichhorn S, Bigler R, Myers EL, Aggarwal VK. Enantiospecific Synthesis of ortho-Substituted Benzylic Boronic Esters by a 1,2-Metalate Rearrangement/1,3-Borotropic Shift Sequence. Journal of the American Chemical Society. PMID 28661133 DOI: 10.1021/Jacs.7B05880 |
0.548 |
|
| 2017 |
Fawcett A, Pradeilles J, Wang Y, Mutsuga T, Myers EL, Aggarwal VK. Photoinduced decarboxylative borylation of carboxylic acids. Science (New York, N.Y.). PMID 28619717 DOI: 10.1126/Science.Aan3679 |
0.416 |
|
| 2017 |
Ganesh V, Odachowski M, Aggarwal VK. Alkynyl Moiety for Triggering 1,2-Metallate Shifts: Enantiospecific sp(2) -sp(3) Coupling of Boronic Esters with p-Arylacetylenes. Angewandte Chemie (International Ed. in English). PMID 28618129 DOI: 10.1002/Anie.201703894 |
0.776 |
|
| 2017 |
Aggarwal VK, Collins B, Wilson C, Myers E. Asymmetric Synthesis of Secondary and Tertiary Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 28525685 DOI: 10.1002/Anie.201701963 |
0.53 |
|
| 2017 |
Armstrong RJ, Niwetmarin W, Aggarwal VK. Synthesis of Functionalized Alkenes by a Transition-Metal-Free Zweifel Coupling. Organic Letters. PMID 28453280 DOI: 10.1021/Acs.Orglett.7B01124 |
0.447 |
|
| 2017 |
Blair DJ, Tanini D, Bateman JM, Scott HK, Myers EL, Aggarwal VK. Selective uni- and bidirectional homologation of diborylmethane. Chemical Science. 8: 2898-2903. PMID 28451355 DOI: 10.1039/C6Sc05338F |
0.492 |
|
| 2017 |
Armstrong RJ, Sandford C, García-Ruiz C, Aggarwal VK. Conjunctive functionalization of vinyl boronate complexes with electrophiles: a diastereoselective three-component coupling. Chemical Communications (Cambridge, England). PMID 28425511 DOI: 10.1039/C7Cc01671A |
0.412 |
|
| 2017 |
Silvi M, Sandford C, Aggarwal VK. Merging Photoredox with 1,2-Metallate Rearrangements: The Photochemical Alkylation of Vinyl Boronate Complexes. Journal of the American Chemical Society. PMID 28402109 DOI: 10.1021/Jacs.7B02569 |
0.797 |
|
| 2017 |
Sandford C, Aggarwal VK. Stereospecific functionalizations and transformations of secondary and tertiary boronic esters. Chemical Communications (Cambridge, England). PMID 28397919 DOI: 10.1039/C7Cc01254C |
0.362 |
|
| 2017 |
Wang Y, Noble A, Sandford C, Aggarwal VK. Enantiospecific Trifluoromethyl-Radical-Induced Three-Component Coupling of Boronic Esters with Furans. Angewandte Chemie (International Ed. in English). PMID 28097819 DOI: 10.1002/Anie.201611058 |
0.478 |
|
| 2017 |
Varela A, Garve LK, Leonori D, Aggarwal VK. Stereocontrolled Total Synthesis of (-)-Stemaphylline. Angewandte Chemie (International Ed. in English). PMID 28097799 DOI: 10.1002/Anie.201611273 |
0.733 |
|
| 2017 |
Carreira EM, Richter MJR, Varela A, Garve LKB, Leonori D, Aggarwal VK. Synthesis of (–)-Stemaphylline Synfacts. 13: 347-2131. DOI: 10.1055/S-0036-1590103 |
0.694 |
|
| 2017 |
Armstrong R, Aggarwal V. 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling Synthesis. 49: 3323-3336. DOI: 10.1055/S-0036-1589046 |
0.504 |
|
| 2017 |
Collins BSL, Wilson CM, Myers EL, Aggarwal VK. Asymmetrische Synthese sekundärer und tertiärer Boronsäureester Angewandte Chemie. 129: 11860-11894. DOI: 10.1002/Ange.201701963 |
0.368 |
|
| 2017 |
Armstrong RJ, Aggarwal VK. Homologation of Boronic Esters with Lithiated Epoxides Organic Syntheses. 94: 234-251. DOI: 10.1002/0471264229.Os094.17 |
0.474 |
|
| 2016 |
Armstrong RJ, García-Ruiz C, Myers EL, Aggarwal VK. Stereodivergent Olefination of Enantioenriched Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 27958668 DOI: 10.1002/Anie.201610387 |
0.492 |
|
| 2016 |
Noble A, Roesner S, Aggarwal VK. Short Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line Synthesis. Angewandte Chemie (International Ed. in English). PMID 27865037 DOI: 10.1002/Anie.201609598 |
0.81 |
|
| 2016 |
Fawcett A, Nitsch D, Ali M, Bateman JM, Myers EL, Aggarwal VK. Regio- and Stereoselective Homologation of 1,2-Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3-Diols and Sch 725674. Angewandte Chemie (International Ed. in English). PMID 27781356 DOI: 10.1002/Anie.201608406 |
0.547 |
|
| 2016 |
Odachowski M, Bonet A, Essafi S, Conti-Ramsden P, Harvey JN, Leonori D, Aggarwal VK. Development of Enantiospecific Coupling of Secondary and Tertiary Boronic Esters with Aromatic Compounds. Journal of the American Chemical Society. PMID 27384259 DOI: 10.1021/Jacs.6B03963 |
0.792 |
|
| 2016 |
Blair DJ, Zhong S, Hesse MJ, Zabaleta N, Myers EL, Aggarwal VK. Full chirality transfer in the synthesis of hindered tertiary boronic esters under in situ lithiation-borylation conditions. Chemical Communications (Cambridge, England). PMID 27002235 DOI: 10.1039/C6Cc00536E |
0.458 |
|
| 2016 |
Wang Y, Noble A, Myers EL, Aggarwal VK. Enantiospecific Alkynylation of Alkylboronic Esters. Angewandte Chemie (International Ed. in English). PMID 26934427 DOI: 10.1002/Anie.201600599 |
0.503 |
|
| 2016 |
Millán A, Smith JR, Aggarwal VK. Tandem Allylboration-Prins Reaction for the Rapid Construction of Substituted Tetrahydropyrans: Application to the Total Synthesis of (-)-Clavosolide A. Angewandte Chemie (International Ed. in English). PMID 26766494 DOI: 10.1002/Anie.201511140 |
0.818 |
|
| 2016 |
Robiette R, Trieu-Van T, Aggarwal VK, Harvey JN. Activation of the SN2 Reaction by Adjacent π Systems: The Critical Role of Electrostatic Interactions and of Dissociative Character. Journal of the American Chemical Society. PMID 26725828 DOI: 10.1021/Jacs.5B11402 |
0.735 |
|
| 2016 |
Casoni G, Myers EL, Aggarwal VK. Synthesis of 3-Aryl-1-aminopropane Derivatives: Lithiation-Borylation-Ring-Opening of Azetidinium Ions Synthesis (Germany). 48: 3241-3253. DOI: 10.1055/S-0035-1562447 |
0.459 |
|
| 2015 |
Roesner S, Blair DJ, Aggarwal VK. Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation-borylation-protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol. Chemical Science. 6: 3718-3723. PMID 29218141 DOI: 10.1039/C4Sc03901G |
0.82 |
|
| 2015 |
Matlock JV, Svejstrup TD, Songara P, Overington S, McGarrigle EM, Aggarwal VK. Synthesis of 6- and 7-Membered N-Heterocycles Using α-Phenylvinylsulfonium Salts. Organic Letters. 17: 5044-7. PMID 26421884 DOI: 10.1021/Acs.Orglett.5B02516 |
0.461 |
|
| 2015 |
Brown CA, Aggarwal VK. Short Convergent Synthesis of the Mycolactone Core Through Lithiation-Borylation Homologations. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 13900-3. PMID 26332797 DOI: 10.1002/Chem.201503122 |
0.436 |
|
| 2015 |
Llaveria J, Leonori D, Aggarwal VK. Stereospecific Coupling of Boronic Esters with N-Heteroaromatic Compounds. Journal of the American Chemical Society. 137: 10958-61. PMID 26292943 DOI: 10.1021/Jacs.5B07842 |
0.7 |
|
| 2015 |
Sandford C, Rasappan R, Aggarwal VK. Synthesis of Enantioenriched Alkylfluorides by the Fluorination of Boronate Complexes. Journal of the American Chemical Society. 137: 10100-3. PMID 26244235 DOI: 10.1021/Jacs.5B05848 |
0.809 |
|
| 2015 |
Feeney K, Berionni G, Mayr H, Aggarwal VK. Structure and reactivity of boron-ate complexes derived from primary and secondary boronic esters. Organic Letters. 17: 2614-7. PMID 25973673 DOI: 10.1021/Acs.Orglett.5B00918 |
0.405 |
|
| 2015 |
Balieu S, Hallett GE, Burns M, Bootwicha T, Studley J, Aggarwal VK. Toward ideality: the synthesis of (+)-kalkitoxin and (+)-hydroxyphthioceranic acid by assembly-line synthesis. Journal of the American Chemical Society. 137: 4398-403. PMID 25625684 DOI: 10.1021/Ja512875G |
0.484 |
|
| 2015 |
Prévost S, Thai K, Schützenmeister N, Coulthard G, Erb W, Aggarwal VK. Synthesis of prostaglandin analogues, latanoprost and bimatoprost, using organocatalysis via a key bicyclic enal intermediate. Organic Letters. 17: 504-7. PMID 25582321 DOI: 10.1021/Ol503520F |
0.458 |
|
| 2015 |
Leonori D, Aggarwal VK. Stereospecific couplings of secondary and tertiary boronic esters. Angewandte Chemie (International Ed. in English). 54: 1082-96. PMID 25414056 DOI: 10.1002/Anie.201407701 |
0.67 |
|
| 2015 |
Knochel P, Haas D, Llaveria J, Leonori D, Aggarwal VK. Stereospecific Coupling of Boronic Esters with Lithiated N-Heterocycles Synfacts. 11: 1197-1197. DOI: 10.1055/S-0035-1560743 |
0.659 |
|
| 2015 |
Unsworth PJ, Löffler LE, Noble A, Aggarwal VK. Palladium-Catalyzed Reactions of Allylic Boronic Esters with Nucleophiles: Novel Umpolung Reactivity Synlett. 26: 1567-1572. DOI: 10.1055/S-0034-1380869 |
0.509 |
|
| 2015 |
Roesner S, Blair DJ, Aggarwal VK. Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation-borylation-protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol Chemical Science. 6: 3718-3723. DOI: 10.1039/c4sc03901g |
0.784 |
|
| 2015 |
Leonori D, Aggarwal VK. Reagent-controlled lithiation–borylation Topics in Organometallic Chemistry. 49: 271-295. DOI: 10.1007/978-3-319-13054-5_9 |
0.691 |
|
| 2014 |
Watson CG, Balanta A, Elford TG, Essafi S, Harvey JN, Aggarwal VK. Construction of multiple, contiguous quaternary stereocenters in acyclic molecules by lithiation-borylation. Journal of the American Chemical Society. 136: 17370-3. PMID 25469619 DOI: 10.1021/Ja509029H |
0.623 |
|
| 2014 |
Essafi S, Tomasi S, Aggarwal VK, Harvey JN. Homologation of boronic esters with organolithium compounds: a computational assessment of mechanism. The Journal of Organic Chemistry. 79: 12148-58. PMID 25318004 DOI: 10.1021/Jo502020E |
0.56 |
|
| 2014 |
Matlock JV, Fritz SP, Harrison SA, Coe DM, McGarrigle EM, Aggarwal VK. Synthesis of α-substituted vinylsulfonium salts and their application as annulation reagents in the formation of epoxide- and cyclopropane-fused heterocycles. The Journal of Organic Chemistry. 79: 10226-39. PMID 25310872 DOI: 10.1021/Jo501885Z |
0.514 |
|
| 2014 |
Leonori D, Aggarwal VK. Lithiation-borylation methodology and its application in synthesis. Accounts of Chemical Research. 47: 3174-83. PMID 25262745 DOI: 10.1021/Ar5002473 |
0.738 |
|
| 2014 |
Burns M, Essafi S, Bame JR, Bull SP, Webster MP, Balieu S, Dale JW, Butts CP, Harvey JN, Aggarwal VK. Assembly-line synthesis of organic molecules with tailored shapes. Nature. 513: 183-8. PMID 25209797 DOI: 10.1038/Nature13711 |
0.544 |
|
| 2014 |
Chen JL, Aggarwal VK. Highly diastereoselective and enantiospecific allylation of ketones and imines using borinic esters: contiguous quaternary stereogenic centers. Angewandte Chemie (International Ed. in English). 53: 10992-6. PMID 25156948 DOI: 10.1002/Anie.201407127 |
0.551 |
|
| 2014 |
Rasappan R, Aggarwal VK. Synthesis of hydroxyphthioceranic acid using a traceless lithiation-borylation-protodeboronation strategy. Nature Chemistry. 6: 810-4. PMID 25143217 DOI: 10.1038/Nchem.2010 |
0.781 |
|
| 2014 |
Unsworth PJ, Leonori D, Aggarwal VK. Stereocontrolled synthesis of 1,5-stereogenic centers through three-carbon homologation of boronic esters. Angewandte Chemie (International Ed. in English). 53: 9846-50. PMID 25044518 DOI: 10.1002/Anie.201405700 |
0.714 |
|
| 2014 |
Bonet A, Odachowski M, Leonori D, Essafi S, Aggarwal VK. Enantiospecific sp(2)-sp(3) coupling of secondary and tertiary boronic esters. Nature Chemistry. 6: 584-9. PMID 24950327 DOI: 10.1038/Nchem.1971 |
0.737 |
|
| 2014 |
Hesse MJ, Essafi S, Watson CG, Harvey JN, Hirst D, Willis CL, Aggarwal VK. Highly selective allylborations of aldehydes using α,α-disubstituted allylic pinacol boronic esters. Angewandte Chemie (International Ed. in English). 53: 6145-9. PMID 24799283 DOI: 10.1002/Anie.201402995 |
0.627 |
|
| 2014 |
Blair DJ, Fletcher CJ, Wheelhouse KM, Aggarwal VK. Stereocontrolled synthesis of adjacent acyclic quaternary-tertiary motifs: application to a concise total synthesis of (-)-filiformin. Angewandte Chemie (International Ed. in English). 53: 5552-5. PMID 24757079 DOI: 10.1002/Anie.201400944 |
0.512 |
|
| 2014 |
Pulis AP, Fackler P, Aggarwal VK. Short stereoselective synthesis of the Phytophthora universal mating hormone α1 using lithiation/borylation reactions. Angewandte Chemie (International Ed. in English). 53: 4382-5. PMID 24634275 DOI: 10.1002/Anie.201400714 |
0.475 |
|
| 2014 |
Roesner S, Brown CA, Mohiti M, Pulis AP, Rasappan R, Blair DJ, Essafi S, Leonori D, Aggarwal VK. Stereospecific conversion of alcohols into pinacol boronic esters using lithiation-borylation methodology with pinacolborane. Chemical Communications (Cambridge, England). 50: 4053-5. PMID 24623123 DOI: 10.1039/C4Cc00993B |
0.825 |
|
| 2014 |
Türkmen YE, Aggarwal VK. A simpler route for making nitrogen-alkene rings. [corrected]. Science (New York, N.Y.). 343: 33-4. PMID 24385622 DOI: 10.1126/Science.1248166 |
0.78 |
|
| 2014 |
Mohiti M, Rampalakos C, Feeney K, Leonori D, Aggarwal VK. Asymmetric addition of chiral boron-ate complexes to cyclic iminium ions Chemical Science. 5: 602-607. DOI: 10.1039/C3Sc52409D |
0.703 |
|
| 2014 |
Leonori D, Aggarwal VK. Stereospezifische Kupplungen von sekundären und tertiären Boronsäureestern Angewandte Chemie. 127: 1096-1111. DOI: 10.1002/Ange.201407701 |
0.606 |
|
| 2014 |
Watson CG, Unsworth PJ, Leonori D, Aggarwal VK. Lithium-Boron Chemistry: A Synergistic Strategy in Modern Synthesis Lithium Compounds in Organic Synthesis: From Fundamentals to Applications. 397-422. DOI: 10.1002/9783527667512.Ch14 |
0.732 |
|
| 2013 |
Chausset-Boissarie L, Ghozati K, LaBine E, Chen JL, Aggarwal VK, Crudden CM. Enantiospecific, regioselective cross-coupling reactions of secondary allylic boronic esters. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 17698-701. PMID 24302640 DOI: 10.1002/Chem.201303683 |
0.415 |
|
| 2013 |
Pulis AP, Blair DJ, Torres E, Aggarwal VK. Synthesis of enantioenriched tertiary boronic esters by the lithiation/borylation of secondary alkyl benzoates. Journal of the American Chemical Society. 135: 16054-7. PMID 24138162 DOI: 10.1021/Ja409100Y |
0.508 |
|
| 2013 |
Arena G, Chen CC, Leonori D, Aggarwal VK. Concise synthesis of (+)-allo-kainic acid via MgI2-mediated tandem aziridine ring opening-formal [3 + 2] cycloaddition. Organic Letters. 15: 4250-3. PMID 23909824 DOI: 10.1021/Ol4020333 |
0.732 |
|
| 2013 |
Illa O, Namutebi M, Saha C, Ostovar M, Chen CC, Haddow MF, Nocquet-Thibault S, Lusi M, McGarrigle EM, Aggarwal VK. Practical and highly selective sulfur ylide-mediated asymmetric epoxidations and aziridinations using a cheap and readily available chiral sulfide: extensive studies to map out scope, limitations, and rationalization of diastereo- and enantioselectivities. Journal of the American Chemical Society. 135: 11951-66. PMID 23902598 DOI: 10.1021/Ja405073W |
0.547 |
|
| 2013 |
Fritz SP, Matlock JV, McGarrigle EM, Aggarwal VK. Efficient synthesis of cyclopropane-fused heterocycles with bromoethylsulfonium salt. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10827-31. PMID 23843399 DOI: 10.1002/Chem.201302081 |
0.465 |
|
| 2013 |
Chen JL, Scott HK, Hesse MJ, Willis CL, Aggarwal VK. Highly diastereo- and enantioselective allylboration of aldehydes using α-substituted allyl/crotyl pinacol boronic esters via in situ generated borinic esters. Journal of the American Chemical Society. 135: 5316-9. PMID 23520993 DOI: 10.1021/Ja401564Z |
0.508 |
|
| 2013 |
Watson CG, Aggarwal VK. Asymmetric synthesis of 1-heteroaryl-1-arylalkyl tertiary alcohols and 1-pyridyl-1-arylethanes by lithiation-borylation methodology. Organic Letters. 15: 1346-9. PMID 23461803 DOI: 10.1021/Ol400289V |
0.44 |
|
| 2013 |
Fletcher CJ, Wheelhouse KM, Aggarwal VK. Stereoselective total synthesis of (+)-giganin and its C10 epimer by using late-stage lithiation-borylation methodology. Angewandte Chemie (International Ed. in English). 52: 2503-6. PMID 23355299 DOI: 10.1002/Anie.201208403 |
0.454 |
|
| 2013 |
Mahmood A, Suárez JR, Thomas SP, Aggarwal VK. One-pot synthesis of 2,3,4,5,6-pentasubstituted tetrahydropyrans using lithiation-borylation, allylation and Prins cyclisation reactions Tetrahedron Letters. 54: 49-51. DOI: 10.1016/J.Tetlet.2012.10.091 |
0.526 |
|
| 2012 |
Roesner S, Aggarwal VK. Enantioselective synthesis of (R)-tolterodine using lithiation/borylation-protodeboronation methodology. Canadian Journal of Chemistry. 90: 965. PMID 23750041 DOI: 10.1139/V2012-069 |
0.794 |
|
| 2012 |
Fritz SP, West TH, McGarrigle EM, Aggarwal VK. Diastereoselective synthesis of CF3-substituted, epoxide-fused heterocycles with β-(trifluoromethyl)vinylsulfonium salts. Organic Letters. 14: 6370-3. PMID 23231752 DOI: 10.1021/Ol303200N |
0.464 |
|
| 2012 |
Hesse MJ, Butts CP, Willis CL, Aggarwal VK. Diastereodivergent synthesis of trisubstituted alkenes through protodeboronation of allylic boronic esters: application to the synthesis of the Californian red scale beetle pheromone. Angewandte Chemie (International Ed. in English). 51: 12444-8. PMID 23129403 DOI: 10.1002/Anie.201207312 |
0.433 |
|
| 2012 |
Partridge BM, Chausset-Boissarie L, Burns M, Pulis AP, Aggarwal VK. Enantioselective synthesis and cross-coupling of tertiary propargylic boronic esters using lithiation-borylation of propargylic carbamates. Angewandte Chemie (International Ed. in English). 51: 11795-9. PMID 23076714 DOI: 10.1002/Anie.201203198 |
0.508 |
|
| 2012 |
Coulthard G, Erb W, Aggarwal VK. Stereocontrolled organocatalytic synthesis of prostaglandin PGF2α in seven steps. Nature. 489: 278-81. PMID 22895192 DOI: 10.1038/Nature11411 |
0.468 |
|
| 2012 |
Roesner S, Aggarwal VK. Organic chemistry: reactions at the end of a tether. Nature. 487: 48-9. PMID 22763453 DOI: 10.1038/Nature11381 |
0.787 |
|
| 2012 |
Aggarwal VK, Ball LT, Carobene S, Connelly RL, Hesse MJ, Partridge BM, Roth P, Thomas SP, Webster MP. Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes. Chemical Communications (Cambridge, England). 48: 9230-2. PMID 22609828 DOI: 10.1039/C2Cc32176A |
0.523 |
|
| 2012 |
Pulis AP, Aggarwal VK. Synthesis of enantioenriched tertiary boronic esters from secondary allylic carbamates. Application to the synthesis of C30 botryococcene. Journal of the American Chemical Society. 134: 7570-4. PMID 22524150 DOI: 10.1021/Ja303022D |
0.563 |
|
| 2012 |
Robinson A, Aggarwal VK. Stereocontrolled asymmetric synthesis of syn-E-1,4-diol-2-enes using allyl boronates and its application in the total synthesis of solandelactone F. Organic & Biomolecular Chemistry. 10: 1795-801. PMID 22258739 DOI: 10.1039/C2Ob06975J |
0.461 |
|
| 2012 |
Ritmaleni R, Aggarwal VK. Attempted Synthesis Of Bis-Spiroepoxide Dithianedioxide Indonesian Journal of Pharmacy. 23: 188-192. DOI: 10.14499/Indonesianjpharm0Iss0Pp188-192 |
0.514 |
|
| 2012 |
Roesner S, Aggarwal VK. Enantioselective synthesis of (R)-tolterodine using lithiation/borylation- protodeboronation methodology Canadian Journal of Chemistry. 90: 965-974. DOI: 10.1139/v2012-069 |
0.741 |
|
| 2012 |
Fritz SP, Moya JF, Unthank MG, Mcgarrigle EM, Aggarwal VK. An efficient synthesis of azetidines with (2-bromoethyl)sulfonium triflate Synthesis. 44: 1584-1590. DOI: 10.1055/S-0031-1290951 |
0.529 |
|
| 2012 |
Pulis AP, Aggarwal VK. Correction to Synthesis of Enantioenriched Tertiary Boronic Esters from Secondary Allylic Carbamates. Application to the Synthesis of C30 Botryococcene Journal of the American Chemical Society. 134: 11298-11298. DOI: 10.1021/Ja304872J |
0.481 |
|
| 2012 |
Fletcher CJ, Blair DJ, Wheelhouse KMP, Aggarwal VK. The total synthesis of (-)-aplysin via a lithiation-borylation- propenylation sequence Tetrahedron. 68: 7598-7604. DOI: 10.1016/J.Tet.2012.05.095 |
0.494 |
|
| 2012 |
Robinson A, Fletcher CJ, Aggarwal VK. Total syntheses of solandelactones E and F Strategies and Tactics in Organic Synthesis. 8: 1-23. DOI: 10.1016/B978-0-12-386540-3.00001-0 |
0.419 |
|
| 2012 |
Fritz SP, Ali Z, Unthank MG, McGarrigle EM, Aggarwal VK. (2-Bromoethyl)sulfonium Trifluoromethanesulfonates in Stereoselective Annulation Reactions for the Formation of Fused Bicyclic Epoxides and Aziridines Helvetica Chimica Acta. 95: 2384-2398. DOI: 10.1002/Hlca.201200455 |
0.543 |
|
| 2012 |
Yar M, Fritz SP, Gates PJ, McGarrigle EM, Aggarwal VK. Synthesis of N-vinyloxazolidinones and morpholines from amino alcohols and vinylsulfonium salts: Analysis of the outcome's dependence on the N-protecting group by nanospray mass spectrometry European Journal of Organic Chemistry. 160-166. DOI: 10.1002/Ejoc.201101272 |
0.414 |
|
| 2012 |
Webster MP, Partridge BM, Aggarwal VK. Lithiated primary alkyl carbamates for the homologation of boronic esters Organic Syntheses. 88: 247-259. DOI: 10.1002/0471264229.Os088.24 |
0.371 |
|
| 2011 |
Scott HK, Aggarwal VK. Highly enantioselective synthesis of tertiary boronic esters and their stereospecific conversion to other functional groups and quaternary stereocentres. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13124-32. PMID 22052475 DOI: 10.1002/Chem.201102581 |
0.502 |
|
| 2011 |
Roesner S, Casatejada JM, Elford TG, Sonawane RP, Aggarwal VK. Enantioselective syntheses of (+)-sertraline and (+)-indatraline using lithiation/borylation-protodeboronation methodology. Organic Letters. 13: 5740-3. PMID 21995597 DOI: 10.1021/Ol202251P |
0.776 |
|
| 2011 |
Larouche-Gauthier R, Elford TG, Aggarwal VK. Ate complexes of secondary boronic esters as chiral organometallic-type nucleophiles for asymmetric synthesis. Journal of the American Chemical Society. 133: 16794-7. PMID 21939203 DOI: 10.1021/Ja2077813 |
0.411 |
|
| 2011 |
Elford TG, Nave S, Sonawane RP, Aggarwal VK. Total synthesis of (+)-erogorgiaene using lithiation-borylation methodology, and stereoselective synthesis of each of its diastereoisomers. Journal of the American Chemical Society. 133: 16798-801. PMID 21936552 DOI: 10.1021/Ja207869F |
0.485 |
|
| 2011 |
Larouche-Gauthier R, Fletcher CJ, Couto I, Aggarwal VK. Use of alkyl 2,4,6-triisopropylbenzoates in the asymmetric homologation of challenging boronic esters. Chemical Communications (Cambridge, England). 47: 12592-4. PMID 21892499 DOI: 10.1039/C1Cc14469C |
0.351 |
|
| 2011 |
Fontana F, Chen CC, Aggarwal VK. Palladium-catalyzed insertion of CO2 into vinylaziridines: new route to 5-vinyloxazolidinones. Organic Letters. 13: 3454-7. PMID 21644531 DOI: 10.1021/Ol201193D |
0.425 |
|
| 2011 |
Lowe MA, Ostovar M, Ferrini S, Chen CC, Lawrence PG, Fontana F, Calabrese AA, Aggarwal VK. Palladium-mediated annulation of vinyl aziridines with Michael acceptors: stereocontrolled synthesis of substituted pyrrolidines and its application in a formal synthesis of (-)-α-kainic acid. Angewandte Chemie (International Ed. in English). 50: 6370-4. PMID 21626630 DOI: 10.1002/Anie.201101389 |
0.502 |
|
| 2011 |
McGarrigle EM, Fritz SP, Favereau L, Yar M, Aggarwal VK. An efficient synthesis of imidazolinium salts using vinyl sulfonium salts. Organic Letters. 13: 3060-3. PMID 21591804 DOI: 10.1021/Ol2009472 |
0.53 |
|
| 2011 |
Sonawane RP, Jheengut V, Rabalakos C, Larouche-Gauthier R, Scott HK, Aggarwal VK. Enantioselective construction of quaternary stereogenic centers from tertiary boronic esters: methodology and applications. Angewandte Chemie (International Ed. in English). 50: 3760-3. PMID 21374774 DOI: 10.1002/Anie.201008067 |
0.431 |
|
| 2011 |
Aggarwal VK, Binanzer M, de Ceglie MC, Gallanti M, Glasspoole BW, Kendrick SJ, Sonawane RP, Vázquez-Romero A, Webster MP. Asymmetric synthesis of tertiary and quaternary allyl- and crotylsilanes via the borylation of lithiated carbamates. Organic Letters. 13: 1490-3. PMID 21332157 DOI: 10.1021/Ol200177F |
0.504 |
|
| 2011 |
Bagutski V, Elford TG, Aggarwal VK. Synthesis of highly enantioenriched C-tertiary amines from boronic esters: application to the synthesis of igmesine. Angewandte Chemie (International Ed. in English). 50: 1080-3. PMID 21268199 DOI: 10.1002/Anie.201006037 |
0.479 |
|
| 2011 |
Yar M, Unthank MG, McGarrigle EM, Aggarwal VK. Remote chiral induction in vinyl sulfonium salt-mediated ring expansion of hemiaminals into epoxide-fused azepines. Chemistry, An Asian Journal. 6: 372-5. PMID 21254413 DOI: 10.1002/Asia.201000817 |
0.436 |
|
| 2011 |
Ritmaleni R, Aggarwal VK. Ring Opening of Spiroepoxides Dithianedioxide with Bis-nucleophiles Journal of Scientific Research. 3: 575-586. DOI: 10.3329/jsr.v3i3.6746 |
0.328 |
|
| 2011 |
Lowe MA, Ostovar M, Ferrini S, Chen CC, Lawrence PG, Fontana F, Calabrese AA, Aggarwal VK. Palladium-Catalyzed Synthesis of Substituted Pyrrolidines Synfacts. 2011: 974-974. DOI: 10.1055/S-0030-1261006 |
0.546 |
|
| 2011 |
Sonawane RP, Jheengut V, Rabalakos C, Larouche-Gauthier R, Scott HK, Aggarwal VK. Construction of Quaternary Stereogenic Centers from TertiaryBoronic Esters Synfacts. 2011: 625-625. DOI: 10.1055/S-0030-1260396 |
0.363 |
|
| 2011 |
Aggarwal VK, Binanzer M, Ceglie MCd, Gallanti M, Glasspoole BW, Kendrick SJF, Sonawane RP, Vázquez-Romero A, Webster MP. Synthesis of Tertiary and Quaternary Allyl- and Crotylsilanes Synfacts. 2011: 654-654. DOI: 10.1055/S-0030-1260360 |
0.507 |
|
| 2011 |
Aggarwal V, Nave S, Sonawane R, Elford T. Asymmetric Synthesis of Tertiary Stereogenic Centers Synfacts. 2011: 0173-0173. DOI: 10.1055/S-0030-1259341 |
0.488 |
|
| 2011 |
Partridge BM, Thomas SP, Aggarwal VK. Enantioenriched synthesis of Escitalopram using lithiation-borylation methodology Tetrahedron. 67: 10082-10088. DOI: 10.1016/J.Tet.2011.09.142 |
0.454 |
|
| 2011 |
Fritz SP, Mumtaz A, Yar M, McGarrigle EM, Aggarwal VK. Sulfinamides as highly effective amine protecting groups and their use in the conversion of Amino alcohols into morpholines European Journal of Organic Chemistry. 3156-3164. DOI: 10.1002/Ejoc.201100337 |
0.436 |
|
| 2011 |
Sonawane RP, Jheengut V, Rabalakos C, Larouche-Gauthier R, Scott HK, Aggarwal VK. Cover Picture: Enantioselective Construction of Quaternary Stereogenic Centers from Tertiary Boronic Esters: Methodology and Applications (Angew. Chem. Int. Ed. 16/2011) Angewandte Chemie International Edition. 50: 3575-3575. DOI: 10.1002/Anie.201101504 |
0.413 |
|
| 2011 |
Sonawane RP, Jheengut V, Rabalakos C, Larouche-Gauthier R, Scott HK, Aggarwal VK. Titelbild: Enantioselective Construction of Quaternary Stereogenic Centers from Tertiary Boronic Esters: Methodology and Applications (Angew. Chem. 16/2011) Angewandte Chemie. 123: 3655-3655. DOI: 10.1002/Ange.201101504 |
0.436 |
|
| 2011 |
Webster MP, Aggarwal VK. Asymmetric Homologation of Boronic Esters with Lithiated Carbamates, Epoxides, and Aziridines Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials (Volume 1 and 2). 2: 479-505. DOI: 10.1002/9783527639328.ch10 |
0.424 |
|
| 2010 |
Nave S, Sonawane RP, Elford TG, Aggarwal VK. Protodeboronation of tertiary boronic esters: asymmetric synthesis of tertiary alkyl stereogenic centers. Journal of the American Chemical Society. 132: 17096-8. PMID 21080646 DOI: 10.1021/Ja1084207 |
0.52 |
|
| 2010 |
Robinson A, Aggarwal VK. Asymmetric total synthesis of solandelactone E: stereocontrolled synthesis of the 2-ene-1,4-diol core through a lithiation-borylation-allylation sequence. Angewandte Chemie (International Ed. in English). 49: 6673-5. PMID 20683835 DOI: 10.1002/Anie.201003236 |
0.375 |
|
| 2010 |
Ros A, Bermejo A, Aggarwal VK. Benzylic boron reagents behaving as allylic boron reagents towards aldehydes: a new asymmetric reaction leading to homoallylic alcohols with concomitant dearomatisation. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 9741-5. PMID 20589854 DOI: 10.1002/Chem.201001174 |
0.655 |
|
| 2010 |
Bagutski V, French RM, Aggarwal VK. Full chirality transfer in the conversion of secondary alcohols into tertiary boronic esters and alcohols using lithiation-borylation reactions. Angewandte Chemie (International Ed. in English). 49: 5142-5. PMID 20544766 DOI: 10.1002/Anie.201001371 |
0.35 |
|
| 2010 |
Riches SL, Saha C, Filgueira NF, Grange E, McGarrigle EM, Aggarwal VK. On the mechanism of ylide-mediated cyclopropanations: evidence for a proton-transfer step and its effect on stereoselectivity. Journal of the American Chemical Society. 132: 7626-30. PMID 20515075 DOI: 10.1021/Ja910631U |
0.428 |
|
| 2010 |
Binanzer M, Fang GY, Aggarwal VK. Asymmetric synthesis of allylsilanes by the borylation of lithiated carbamates: formal total synthesis of (-)-decarestrictine D. Angewandte Chemie (International Ed. in English). 49: 4264-8. PMID 20446329 DOI: 10.1002/Anie.201001223 |
0.421 |
|
| 2010 |
Althaus M, Mahmood A, Suárez JR, Thomas SP, Aggarwal VK. Application of the lithiation-borylation reaction to the preparation of enantioenriched allylic boron reagents and subsequent in situ conversion into 1,2,4-trisubstituted homoallylic alcohols with complete control over all elements of stereochemistry. Journal of the American Chemical Society. 132: 4025-8. PMID 20192266 DOI: 10.1021/Ja910593W |
0.481 |
|
| 2010 |
Illa O, Arshad M, Ros A, McGarrigle EM, Aggarwal VK. Practical and highly selective sulfur ylide mediated asymmetric epoxidations and aziridinations using an inexpensive, readily available chiral sulfide. Applications to the synthesis of quinine and quinidine. Journal of the American Chemical Society. 132: 1828-30. PMID 20102201 DOI: 10.1021/Ja9100276 |
0.735 |
|
| 2010 |
Fontana F, Tron GC, Barbero N, Ferrini S, Thomas SP, Aggarwal VK. Stereoselective synthesis of trans-beta-lactams by palladium-catalysed carbonylation of vinyl aziridines. Chemical Communications (Cambridge, England). 46: 267-9. PMID 20024347 DOI: 10.1039/B920564K |
0.359 |
|
| 2010 |
Namutebi M, McGarrigle EM, Aggarwal VK. Ring-opening of NH-aziridines with thiols in ionic liquids: Application to the synthesis of aminosulfide catalysts for asymmetric epoxidation of aldehydes Phosphorus, Sulfur and Silicon and the Related Elements. 185: 1250-1272. DOI: 10.1080/10426501003773787 |
0.528 |
|
| 2010 |
Aggarwal V, Binanzer M, Fang G. Synthesis of (-)-Decarestrictine D Synfacts. 2010: 1097-1097. DOI: 10.1055/S-0030-1258622 |
0.313 |
|
| 2010 |
Fontana F, Tron GC, Barbero N, Ferrini S, Thomas SP, Aggarwal VK. Palladium-Catalyzed Synthesis of β-Lactams by Carbonylationof Vinyl Aziridines Synfacts. 2010: 405-405. DOI: 10.1055/S-0029-1219505 |
0.409 |
|
| 2010 |
Killen JC, Leonard J, Aggarwal VK. A novel asymmetric azaspirocyclisation using a Morita-Baylis-Hillman-type reaction Synlett. 579-582. DOI: 10.1055/S-0029-1219210 |
0.442 |
|
| 2010 |
Arshad M, Fernández MA, McGarrigle EM, Aggarwal VK. Synthesis of quinine and quinidine using sulfur ylide-mediated asymmetric epoxidation as a key step Tetrahedron Asymmetry. 21: 1771-1776. DOI: 10.1016/J.Tetasy.2010.04.046 |
0.555 |
|
| 2010 |
Kitulagoda JE, Palmelund A, Aggarwal VK. Synthesis of highly functionalized 2,5-disubstituted pyrrolidines via an aza-Morita-Baylis-Hillman-type reaction Tetrahedron. 66: 6293-6299. DOI: 10.1016/J.Tet.2010.05.047 |
0.495 |
|
| 2010 |
Kitulagoda JE, Palmelund A, Aggarwal VK. ChemInform Abstract: Synthesis of Highly Functionalized 2,5-Disubstituted Pyrrolidines via an aza-Morita-Baylis-Hillman-Type Reaction. Cheminform. 42: no-no. DOI: 10.1002/chin.201101088 |
0.374 |
|
| 2010 |
Aggarwal VK, Patel M, Studley J. ChemInform Abstract: Synthesis of Epoxides from Aldehydes and Tosylhydrazone Salts Catalyzed by Triphenylarsine: Complete trans Selectivity for all Combinations of Coupling Partners. Cheminform. 33: no-no. DOI: 10.1002/chin.200244120 |
0.392 |
|
| 2010 |
Aggarwal VK, Alonso E, Ferrara M, Spey SE. ChemInform Abstract: Highly Diastereoselective Aziridination of Imines with Trimethylsilyldiazomethane. Subsequent Silyl Substitution with Electrophiles, Ring Opening, and Metalation of C-Silylaziridines - A Cornucopia of Highly Selective Transformations. Cheminform. 33: no-no. DOI: 10.1002/chin.200237106 |
0.303 |
|
| 2010 |
Aggarwal VK, Coogan MP, Stenson RA, Jones RVH, Fieldhouse R, Blacker J. ChemInform Abstract: Developments in the Simmons - Smith-Mediated Epoxidation Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200224055 |
0.31 |
|
| 2010 |
Aggarwal VK, Ferrara M, O'Brien CJ, Thompson A, Jones RVH, Fieldhouse R. ChemInform Abstract: Scope and Limitations in Sulfur Ylide Mediated Catalytic Asymmetric Aziridination of Imines: Use of Phenyldiazomethane, Diazoesters, and Diazoacetamides. Cheminform. 32: no-no. DOI: 10.1002/chin.200147087 |
0.59 |
|
| 2010 |
Aggarwal VK, Smith HW, Hynd G, Jones RVH, Fieldhouse R, Spey SE. ChemInform Abstract: Catalytic Cyclopropanation of Electron Deficient Alkenes Mediated by Chiral and Achiral Sulfides: Scope and Limitations in Reactions Involving Phenyldiazomethane and Ethyl Diazoacetate. Cheminform. 32: no-no. DOI: 10.1002/chin.200107046 |
0.358 |
|
| 2010 |
Aggarwal VK. ChemInform Abstract: Epoxide Formation of Enones and Aldehydes Cheminform. 31: no-no. DOI: 10.1002/chin.200018186 |
0.335 |
|
| 2010 |
Aggarwal VK, Bethel PA, Giles R. ChemInform Abstract: A Formal Synthesis of (+)-Pyripyropene A Using a Biomimetic Epoxy-Olefin Cyclization: Effect of Epoxy Alcohol/Ether on Cyclization Efficiency. Cheminform. 31: no-no. DOI: 10.1002/chin.200013213 |
0.327 |
|
| 2010 |
Aggarwal VK, Ferrara M, Hainz R, Spey SE. ChemInform Abstract: [2,3]-Sigmatropic Rearrangement of Allylic Sulfur Ylides Derived from Trimethylsilyldiazomethane (TMSD). Cheminform. 31: no-no. DOI: 10.1002/chin.200009168 |
0.354 |
|
| 2010 |
Aggarwal VK, Humphries PS, Fenwick A. ChemInform Abstract: Enantioselective Deprotonation of 4-tert-Butylcyclohexanone by Conformationally Constrained Chiral Lithium Amide Bases. Cheminform. 31: no-no. DOI: 10.1002/chin.200005035 |
0.341 |
|
| 2010 |
Aggarwal VK, Barrell JK, Worrall JM, Alexander R. ChemInform Abstract: Highly Diastereoselective Epoxidation of Ketene Dithioacetal Dioxides: A New Approach to the Asymmetric Synthesis of α-Amino Amides. Cheminform. 30: no-no. DOI: 10.1002/chin.199913133 |
0.321 |
|
| 2010 |
Aggarwal VK, Vennall GP. ChemInform Abstract: Sc(OTf)3, an Efficient Catalyst for Addition of Allyltrimethylsilane to Aldehydes; Chemoselective Addition to Aldehydes in Presence of Ketones and in situ Acylation (3 Component Coupling) Cheminform. 30: no-no. DOI: 10.1002/chin.199908309 |
0.319 |
|
| 2010 |
AGGARWAL VK, BLACKSBURN P, FIELDHOUSE R, JONES RVH. ChemInform Abstract: Catalytic Sulfur Ylide Reactions: Use of Diazoacetamides for the Diastereoselective Synthesis of Glycidic Amides. Cheminform. 30: no-no. DOI: 10.1002/chin.199906095 |
0.429 |
|
| 2010 |
AGGARWAL VK, ANDERSON ES, JONES DE, OBIEREY KB, GILES R. ChemInform Abstract: Catalytic Asymmetric Diels-Alder Reactions of α-Thioacrylates for the Preparation of Norbornenone. Cheminform. 30: no-no. DOI: 10.1002/chin.199901034 |
0.336 |
|
| 2010 |
AGGARWAL VK, FONQUERNA S, VENNALL GP. ChemInform Abstract: Sc(OTf)3, an Efficient Catalyst for Formation and Deprotection of Geminal Diacetates (Acylals); Chemoselective Protection of Aldehydes in Presence of Ketones. Cheminform. 29: no-no. DOI: 10.1002/chin.199847076 |
0.311 |
|
| 2010 |
AGGARWAL VK, FORD JG, JONES RVH, FIELDHOUSE R. ChemInform Abstract: Camphor-Derived 1,4-Oxathianes for Carbonyl Epoxidation. Cheminform. 29: no-no. DOI: 10.1002/chin.199840097 |
0.311 |
|
| 2010 |
AGGARWAL VK, GRAINGER RS, ADAMS H, SPARGO PL. ChemInform Abstract: 1,3-Dipolar Cycloaddition Reactions of trans-2-Methylene-1,3-dithiolane 1,3-Dioxide with Nitrones. Cheminform. 29: no-no. DOI: 10.1002/chin.199837146 |
0.342 |
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| 2010 |
AGGARWAL VK, VENNALL GP, DAVEY PN, NEWMAN C. ChemInform Abstract: Scandium Trifluoromethanesulfonate, an Efficient Catalyst for the Intermolecular Carbonyl-Ene Reaction and the Intramolecular Cyclization of Citronellal. Cheminform. 29: no-no. DOI: 10.1002/chin.199827104 |
0.352 |
|
| 2010 |
AGGARWAL VK, ALI A, COOGAN MP. ChemInform Abstract: A Novel Procedure for the Synthesis of Epoxides: Application of Simmons-Smith Reagents Toward Epoxidation. Cheminform. 29: no-no. DOI: 10.1002/chin.199819103 |
0.322 |
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| 2010 |
AGGARWAL VK, THOMAS A, SCHADE S. ChemInform Abstract: trans-1,3-Dithiane-1,3-dioxide: A Chiral Acyl Anion Equivalent. Enantioselective Synthesis of α-Hydroxy-carboxylic Acids, Esters, Amides, and Ketones. Cheminform. 29: no-no. DOI: 10.1002/chin.199812123 |
0.384 |
|
| 2010 |
LI A, DAI L, AGGARWAL VK. ChemInform Abstract: Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement Cheminform. 28: no-no. DOI: 10.1002/chin.199752316 |
0.394 |
|
| 2010 |
AGGARWAL VK, MONTEIRO N. ChemInform Abstract: Asymmetric Total Synthesis of (+)-Carbocyclic Uracil Polyoxin C. Cheminform. 28: no-no. DOI: 10.1002/chin.199751251 |
0.305 |
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| 2010 |
AGGARWAL VK, MONTEIRO N, TARVER GJ, MCCAGUE R. ChemInform Abstract: Scope and Limitations in Palladium-Catalyzed Substitution Reactions of Unsaturated Fused Lactones. Cheminform. 28: no-no. DOI: 10.1002/chin.199749131 |
0.412 |
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| 2010 |
AGGARWAL VK, VENNALL GP, DAVEY PN, NEWMAN C. ChemInform Abstract: Trifluoromethanesulfonic Acid, an Efficient Catalyst for the Hetero Diels-Alder Reaction and an Improved Synthesis of Mefrosol. Cheminform. 28: no-no. DOI: 10.1002/chin.199730131 |
0.359 |
|
| 2010 |
AGGARWAL VK, SCHADE S, ADAMS H. ChemInform Abstract: Anion Reactions of trans-1,3-Dithiolane 1,3-Dioxide with Aldehydes and Comparison with trans-1,3-Dithiane 1,3-Dioxide. Cheminform. 28: no-no. DOI: 10.1002/chin.199727135 |
0.327 |
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| 2010 |
AGGARWAL VK, BOCCARDO G, WORRALL JM, ADAMS H, ALEXANDER R. ChemInform Abstract: 2-Halogeno-1,3-dithiane 1,3-Dioxide: A Diastereoselective Carbonyl Anion Equivalent in Reactions with Aldehydes. Cheminform. 28: no-no. DOI: 10.1002/chin.199721162 |
0.375 |
|
| 2010 |
AGGARWAL VK, THOMPSON A, JONES RVH, STANDEN MCH. ChemInform Abstract: Novel Catalytic and Asymmetric Process for Aziridination Mediated by Sulfur Ylides. Cheminform. 28: no-no. DOI: 10.1002/chin.199717086 |
0.579 |
|
| 2010 |
AGGARWAL VK, ABDEL-RAHMAN H, FAN L, JONES RVH, STANDEN MCH. ChemInform Abstract: A Novel Catalytic Cycle for the Synthesis of Epoxides Using Sulfur Ylides. Cheminform. 27: no-no. DOI: 10.1002/chin.199646114 |
0.362 |
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| 2010 |
AGGARWAL VK, FORD JG, THOMPSON A, JONES RVH, STANDEN MCH. ChemInform Abstract: Direct Asymmetric Epoxidation of Aldehydes Using Catalytic Amounts of Enantiomerically Pure Sulfides. Cheminform. 27: no-no. DOI: 10.1002/chin.199645054 |
0.635 |
|
| 2010 |
AGGARWAL VK, MONTEIRO N, TARVER GJ, LINDELL SD. ChemInform Abstract: Palladium-Catalyzed Substitution of Unsaturated Lactones. Application to the Synthesis of Carbocyclic Polyoxins and Nikkomycins. Cheminform. 27: no-no. DOI: 10.1002/chin.199630054 |
0.449 |
|
| 2010 |
AGGARWAL VK, WANG MF. ChemInform Abstract: Catalytic Asymmetric Synthesis of Epoxides Mediated by Chiral Iminium Salts. Cheminform. 27: no-no. DOI: 10.1002/chin.199622070 |
0.405 |
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| 2010 |
AGGARWAL VK, THOMPSON A, JONES RVH, STANDEN M. ChemInform Abstract: The Use of Chiral Sulfides in Catalytic Asymmetric Epoxidation. Cheminform. 27: no-no. DOI: 10.1002/chin.199611050 |
0.596 |
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| 2010 |
AGGARWAL VK, FRANKLIN R, MADDOCK J, EVANS GR, THOMAS A, MAHON MF, MOLLOY KC, RICE MJ. ChemInform Abstract: Anion Reactions of 1,3-Dithiane 1,3-Dioxide with Carbonyl Compounds: High Diastereoselectivity with Aromatic Aldehydes under Conditions of Equilibrium Control. Cheminform. 26: no-no. DOI: 10.1002/chin.199534174 |
0.325 |
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| 2010 |
AGGARWAL VK, WORRALL JM, ADAMS H, ALEXANDER R. ChemInform Abstract: Stereoselective Addition Reactions of Lithiated 2-Chloro-1,3-dithiane- 1,3-dioxide to Aldehydes. Cheminform. 26: no-no. DOI: 10.1002/chin.199501169 |
0.383 |
|
| 2010 |
AGGARWAL VK, THOMAS A, FRANKLIN RJ. ChemInform Abstract: trans-1,3-Dithiane-1,3-dioxide, a New Chiral Acyl Anion Equivalent for the Preparation of Masked Activated Acids: Application to the Synthesis of α-Hydroxy Acid Derivatives. Cheminform. 25: no-no. DOI: 10.1002/chin.199449141 |
0.322 |
|
| 2010 |
AGGARWAL VK, ABDEL-RAHMAN H, JONES RVH, LEE HY, REID BD. ChemInform Abstract: Novel Catalytic Cycle for the Synthesis of Epoxides from Aldehydes and Sulfur Ylides Mediated by Catalytic Quantities of Sulfides and Rh2(OAc) 4. Cheminform. 25: no-no. DOI: 10.1002/chin.199449065 |
0.389 |
|
| 2010 |
AGGARWAL VK, KALOMIRI M, THOMAS AP. ChemInform Abstract: Asymmetric Epoxidation Using Chiral Sulfur Ylides. Cheminform. 25: no-no. DOI: 10.1002/chin.199435079 |
0.324 |
|
| 2010 |
AGGARWAL VK, LIGHTOWLER M. ChemInform Abstract: Chiral Ketene Equivalents for Use in Asymmetric Synthesis Cheminform. 24: no-no. DOI: 10.1002/chin.199323060 |
0.36 |
|
| 2010 |
AGGARWAL VK, FRANKLIN RJ, RICE MJ. ChemInform Abstract: Highly Stereoselective Addition Reactions of Metalated trans-1,3- Dithiane 1,3-Dioxide to Aldehydes. Cheminform. 23: no-no. DOI: 10.1002/chin.199231200 |
0.323 |
|
| 2010 |
AGGARWAL VK, COLDHAM I, MCINTYRE S, WARREN S. ChemInform Abstract: Transformation of Cyclic α-Phenylthio Aldehydes by Stereoselective Aldol Reactions and Phenylthio Migration into Spirocyclic Lactones and Ethers, and E-Allylic Alcohols with 1,4- Related Chiral Centers. Cheminform. 22: no-no. DOI: 10.1002/chin.199118136 |
0.346 |
|
| 2009 |
Aggarwal VK. Organic synthesis: New uses for old building blocks. Nature Chemistry. 1: 433-4. PMID 21378909 DOI: 10.1038/Nchem.346 |
0.463 |
|
| 2009 |
Ros A, Aggarwal VK. Complete stereoretention in the rhodium-catalyzed 1,2-addition of chiral secondary and tertiary alkyl potassium trifluoroborate salts to aldehydes. Angewandte Chemie (International Ed. in English). 48: 6289-92. PMID 19585631 DOI: 10.1002/Anie.200901900 |
0.716 |
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| 2009 |
Dutheuil G, Webster MP, Worthington PA, Aggarwal VK. Stereocontrolled synthesis of carbon chains bearing contiguous methyl groups by iterative boronic ester homologations: application to the total synthesis of (+)-faranal. Angewandte Chemie (International Ed. in English). 48: 6317-9. PMID 19437526 DOI: 10.1002/Anie.200901194 |
0.427 |
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| 2009 |
Thomas SP, French RM, Jheengut V, Aggarwal VK. Homologation and alkylation of boronic esters and boranes by 1,2-metallate rearrangement of boronate complexes. Chemical Record (New York, N.Y.). 9: 24-39. PMID 19243084 DOI: 10.1002/Tcr.20168 |
0.532 |
|
| 2009 |
Thomas SP, Aggarwal VK. Asymmetric hydroboration of 1,1-disubstituted alkenes. Angewandte Chemie (International Ed. in English). 48: 1896-8. PMID 19185046 DOI: 10.1002/Anie.200805604 |
0.429 |
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| 2009 |
Schmidt F, Keller F, Vedrenne E, Aggarwal VK. Stereocontrolled synthesis of beta-amino alcohols from lithiated aziridines and boronic esters. Angewandte Chemie (International Ed. in English). 48: 1149-52. PMID 19115354 DOI: 10.1002/Anie.200805272 |
0.339 |
|
| 2009 |
Yar M, McGarrigle EM, Aggarwal VK. Bromoethylsulfonium salt--a more effective annulation agent for the synthesis of 6- and 7-membered 1,4-heterocyclic compounds. Organic Letters. 11: 257-60. PMID 19072319 DOI: 10.1021/Ol8023727 |
0.506 |
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| 2009 |
Vedrenne E, Wallner OA, Vitale M, Schmidt F, Aggarwal VK. Homologation of boronic esters with lithiated epoxides for the stereocontrolled synthesis of 1,2- and 1,3-diols and 1,2,4-triols. Organic Letters. 11: 165-8. PMID 19067552 DOI: 10.1021/Ol802651B |
0.79 |
|
| 2009 |
Dutheuil G, Webster MP, Worthington PA, Aggarwal VK. An Iterative Approach to the Total Synthesis of (+)-Faranal Synfacts. 2009: 1134-1134. DOI: 10.1055/S-0029-1217846 |
0.361 |
|
| 2009 |
Schmidt F, Keller F, Vedrenne E, Aggarwal VK. Stereo- and Regioselective Synthesis of Amino Alcohols viaLithiation/Borylation of Aziridines Synfacts. 2009: 438-438. DOI: 10.1055/S-0028-1087831 |
0.36 |
|
| 2009 |
Aggarwal V, Stymiest J, Bagutski V, French R. Enantiodivergent Synthesis of Tertiary Alcohols from Secondary Carbamates Synfacts. 2009: 0284-0284. DOI: 10.1055/S-0028-1087778 |
0.327 |
|
| 2009 |
Aggarwal VK, Barbero N, McGarrigle EM, Mickle G, Navas R, Suárez JR, Unthank MG, Yar M. The fate of the tert-butylsulfinyl auxiliary after acid-promoted cleavage-a method for recycling t-BuSONH2 Tetrahedron Letters. 50: 3482-3484. DOI: 10.1016/J.Tetlet.2009.03.020 |
0.401 |
|
| 2009 |
Bagutski V, Ros A, Aggarwal VK. Improved method for the conversion of pinacolboronic esters into trifluoroborate salts: facile synthesis of chiral secondary and tertiary trifluoroborates Tetrahedron. 65: 9956-9960. DOI: 10.1016/J.Tet.2009.10.002 |
0.693 |
|
| 2009 |
Dutheuil G, Webster M, Worthington P, Aggarwal V. Innentitelbild: Stereocontrolled Synthesis of Carbon Chains Bearing Contiguous Methyl Groups by Iterative Boronic Ester Homologations: Application to the Total Synthesis of (+)-Faranal (Angew. Chem. 34/2009) Angewandte Chemie. 121: 6292-6292. DOI: 10.1002/Ange.200990178 |
0.427 |
|
| 2009 |
Aggarwal VK, Sommer K. Rearrangements of Organozinc Compounds Patai's Chemistry of Functional Groups. 595-639. DOI: 10.1002/9780470682531.Pat0376 |
0.367 |
|
| 2008 |
Stymiest JL, Bagutski V, French RM, Aggarwal VK. Enantiodivergent conversion of chiral secondary alcohols into tertiary alcohols. Nature. 456: 778-82. PMID 19079057 DOI: 10.1038/Nature07592 |
0.338 |
|
| 2008 |
Hansch M, Illa O, McGarrigle EM, Aggarwal VK. Synthesis and application of easily recyclable thiomorpholines for use in sulfur ylide mediated asymmetric epoxidation of aldehydes. Chemistry, An Asian Journal. 3: 1657-63. PMID 18604816 DOI: 10.1002/Asia.200800174 |
0.489 |
|
| 2008 |
Yar M, McGarrigle EM, Aggarwal VK. An annulation reaction for the synthesis of morpholines, thiomorpholines, and piperazines from beta-heteroatom amino compounds and vinyl sulfonium salts. Angewandte Chemie (International Ed. in English). 47: 3784-6. PMID 18404756 DOI: 10.1002/Anie.200800373 |
0.409 |
|
| 2008 |
Bi J, Aggarwal VK. Application of furyl-stabilized sulfur ylides to a concise synthesis of 8a-epi-swainsonine. Chemical Communications (Cambridge, England). 120-2. PMID 18399420 DOI: 10.1039/B713447A |
0.39 |
|
| 2008 |
Howells D, Robiette R, Fang GY, Knowles LS, Woodrow MD, Harvey JN, Aggarwal VK. Reactions of silyl-stabilised sulfur ylides with organoboranes: enantioselectivity, mechanism, and understanding. Organic & Biomolecular Chemistry. 6: 1185-9. PMID 18362956 DOI: 10.1039/B718496D |
0.76 |
|
| 2008 |
Unthank MG, Tavassoli B, Aggarwal VK. Epoxy-annulations by reactions of alpha-amido ketones with vinyl sulfonium salts. Reagent versus substrate control and kinetic resolution. Organic Letters. 10: 1501-4. PMID 18336037 DOI: 10.1021/Ol800318H |
0.477 |
|
| 2008 |
Coldham I, Patel JJ, Raimbault S, Whittaker DT, Adams H, Fang GY, Aggarwal VK. Asymmetric lithiation-substitution of amines involving rearrangement of borates. Organic Letters. 10: 141-3. PMID 18069845 DOI: 10.1021/Ol702734U |
0.416 |
|
| 2008 |
Kokotos CG, McGarrigle EM, Aggarwal VK. Sulfur ylide mediated three-component aziridination and epoxidation reactions using vinyl sulfonium salts Synlett. 2191-2195. DOI: 10.1055/S-2008-1078252 |
0.454 |
|
| 2008 |
Dutheuil G, Selander N, Szabó KJ, Aggarwal VK. Direct synthesis of functionalized allylic boronic esters from allylic alcohols and inexpensive reagents and catalysts Synthesis. 2293-2297. DOI: 10.1055/S-2008-1067144 |
0.411 |
|
| 2008 |
Aggarwal V, Kokotos C, McGarrigle E. Three-Component Synthesis of Epoxides and Aziridines via Sulfur Ylides Synfacts. 2008: 1142-1142. DOI: 10.1055/S-0028-1083487 |
0.44 |
|
| 2007 |
McGarrigle EM, Myers EL, Illa O, Shaw MA, Riches SL, Aggarwal VK. Chalcogenides as organocatalysts. Chemical Reviews. 107: 5841-83. PMID 18072810 DOI: 10.1021/Cr068402Y |
0.3 |
|
| 2007 |
Robiette R, Aggarwal VK, Harvey JN. Mechanism of the Morita-Baylis-Hillman reaction: a computational investigation. Journal of the American Chemical Society. 129: 15513-25. PMID 18041831 DOI: 10.1021/Ja0717865 |
0.753 |
|
| 2007 |
Fang GY, Wallner OA, Di Blasio N, Ginesta X, Harvey JN, Aggarwal VK. Asymmetric sulfur ylide reactions with boranes: scope and limitations, mechanism and understanding. Journal of the American Chemical Society. 129: 14632-9. PMID 17985887 DOI: 10.1021/Ja074110I |
0.659 |
|
| 2007 |
Palmelund A, Myers EL, Tai LR, Tisserand S, Butts CP, Aggarwal VK. A new manifold for the Morita reaction: diene synthesis from simple aldehydes and acrylates/acrylonitrile mediated by phosphines. Chemical Communications (Cambridge, England). 4128-30. PMID 17925951 DOI: 10.1039/B709157E |
0.529 |
|
| 2007 |
Stymiest JL, Dutheuil G, Mahmood A, Aggarwal VK. Lithiated carbamates: chiral carbenoids for iterative homologation of boranes and boronic esters. Angewandte Chemie (International Ed. in English). 46: 7491-4. PMID 17659521 DOI: 10.1002/Anie.200702146 |
0.442 |
|
| 2007 |
Kokotos CG, Aggarwal VK. Aminals as substrates for sulfur ylides: a synthesis of functionalized aziridines and N-heterocycles. Organic Letters. 9: 2099-102. PMID 17465558 DOI: 10.1021/Ol070507F |
0.489 |
|
| 2007 |
Myers EL, de Vries JG, Aggarwal VK. Reactions of iminium ions with Michael acceptors through a Morita-Baylis-Hillman-type reaction: enantiocontrol and applications in synthesis. Angewandte Chemie (International Ed. in English). 46: 1893-6. PMID 17278162 DOI: 10.1002/Anie.200604715 |
0.42 |
|
| 2007 |
Fang GY, Aggarwal VK. Asymmetric synthesis of alpha-substituted allyl boranes and their application in the synthesis of iso-agatharesinol. Angewandte Chemie (International Ed. in English). 46: 359-62. PMID 17146825 DOI: 10.1002/Anie.200603659 |
0.432 |
|
| 2007 |
Moorthie VA, McGarrigle EM, Stenson R, Aggarwal VK. Studies towards a biomimetic synthesis of α-cyclopiazonic acid: Synthesis of 5-substituted isoxazole-4-carboxylic esters Arkivoc. 2007: 139-151. DOI: 10.3998/Ark.5550190.0008.512 |
0.547 |
|
| 2007 |
Aggarwal V, Fang G. Synthesis of Iso-agatharesinol Synfacts. 2007: 0464-0464. DOI: 10.1055/s-2007-968395 |
0.35 |
|
| 2007 |
Aggarwal V, Unthank M, Hussain N. Formal Synthesis of (-)-Balanol Synfacts. 2007: 0239-0239. DOI: 10.1055/S-2007-968199 |
0.452 |
|
| 2007 |
Stymiest J, Dutheuil G, Mahmood A, Aggarwal V. Cover Picture: Lithiated Carbamates: Chiral Carbenoids for Iterative Homologation of Boranes and Boronic Esters (Angew. Chem. Int. Ed. 39/2007) Angewandte Chemie International Edition. 46: 7333-7333. DOI: 10.1002/Anie.200790193 |
0.42 |
|
| 2007 |
Stymiest J, Dutheuil G, Mahmood A, Aggarwal V. Titelbild: Lithiated Carbamates: Chiral Carbenoids for Iterative Homologation of Boranes and Boronic Esters (Angew. Chem. 39/2007) Angewandte Chemie. 119: 7475-7475. DOI: 10.1002/Ange.200790193 |
0.442 |
|
| 2006 |
Badine DM, Hebach C, Aggarwal VK. Readily synthesized chiral sulfides as reagents for asymmetric epoxidation. Chemistry, An Asian Journal. 1: 438-44. PMID 17441080 DOI: 10.1002/Asia.200600079 |
0.473 |
|
| 2006 |
Unthank MG, Hussain N, Aggarwal VK. The use of vinyl sulfonium salts in the stereocontrolled asymmetric synthesis of epoxide- and aziridine-fused heterocycles: application to the synthesis of (-)-balanol. Angewandte Chemie (International Ed. in English). 45: 7066-9. PMID 17009383 DOI: 10.1002/Anie.200602782 |
0.5 |
|
| 2006 |
Kokotos CG, Aggarwal VK. Hemiaminals as substrates for sulfur ylides: direct asymmetric syntheses of functionalised pyrrolidines and piperidines. Chemical Communications (Cambridge, England). 2156-8. PMID 16703139 DOI: 10.1039/B602226J |
0.518 |
|
| 2006 |
Vitale M, Lecourt T, Sheldon CG, Aggarwal VK. Ligand-induced control of C-H versus aliphatic C-C migration reactions of Rh carbenoids. Journal of the American Chemical Society. 128: 2524-5. PMID 16492022 DOI: 10.1021/Ja057739Z |
0.713 |
|
| 2006 |
Robiette R, Richardson J, Aggarwal VK, Harvey JN. Reactivity and selectivity in the Wittig reaction: a computational study. Journal of the American Chemical Society. 128: 2394-409. PMID 16478195 DOI: 10.1021/Ja056650Q |
0.723 |
|
| 2006 |
Robiette R, Conza M, Aggarwal VK. Delineation of the factors governing reactivity and selectivity in epoxide formation from ammonium ylides and aldehydes. Organic & Biomolecular Chemistry. 4: 621-3. PMID 16467935 DOI: 10.1039/B516926G |
0.718 |
|
| 2006 |
Robiette R, Fang GY, Harvey JN, Aggarwal VK. Is phenyl a good migrating group in the rearrangement of organoborates generated from sulfur ylides? Chemical Communications (Cambridge, England). 741-3. PMID 16465325 DOI: 10.1039/B514987H |
0.749 |
|
| 2006 |
Aggarwal VK, Charmant JP, Fuentes D, Harvey JN, Hynd G, Ohara D, Picoul W, Robiette R, Smith C, Vasse JL, Winn CL. Highly enantioselective synthesis of glycidic amides using camphor-derived sulfonium salts. Mechanism and applications in synthesis. Journal of the American Chemical Society. 128: 2105-14. PMID 16464113 DOI: 10.1021/Ja0568345 |
0.809 |
|
| 2006 |
Florio S, Aggarwal V, Salomone A. Lithiation and reactions of stilbene oxides: synthetic utility. Organic Letters. 6: 4191-4. PMID 15524440 DOI: 10.1021/Ol0485013 |
0.302 |
|
| 2006 |
Aggarwal VK, Fang GY, Ginesta X, Howells DM, Zaja M. Toward an understanding of the factors responsible for the 1,2-migration of alkyl groups in borate complexes Pure and Applied Chemistry. 78: 215-229. DOI: 10.1351/Pac200678020215 |
0.418 |
|
| 2006 |
Aggarwal V, Charmant J, Fuentes D, Harvey J, Hynd G, Ohara D, Picoul W, Robiette R, Smith C, Vasse J, Winn C. Synthesis of SK&F 104353 Synfacts. 2006: 0633-0633. DOI: 10.1055/S-2006-941825 |
0.697 |
|
| 2006 |
Aggarwal VK, Staubitz AC, Owen M. Optimization of the Mizoroki-Heck reaction using Design of Experiment (DoE) Organic Process Research and Development. 10: 64-69. DOI: 10.1021/Op058013Q |
0.359 |
|
| 2006 |
Aggarwal VK, Fang G, Kokotos CG, Richardson J, Unthank MG. A practical synthesis of a [2.2.1] bicyclic chiral sulfide for asymmetric transformations Tetrahedron. 62: 11297-11303. DOI: 10.1016/J.Tet.2006.06.044 |
0.45 |
|
| 2006 |
Harvey JN, Aggarwal VK, Bathelt CM, Carreón-Macedo JL, Gallagher T, Holzmann N, Mulholland AJ, Robiette R. QM and QM/MM studies of selectivity in organic and bioorganic chemistry Journal of Physical Organic Chemistry. 19: 608-615. DOI: 10.1002/Poc.1030 |
0.741 |
|
| 2006 |
Aggarwal VK, Badine DM, Moorthie VA. Asymmetric Synthesis of Epoxides and Aziridines from Aldehydes and Imines Aziridines and Epoxides in Organic Synthesis. 1-35. DOI: 10.1002/3527607862.ch1 |
0.45 |
|
| 2005 |
Aggarwal VK, Bi J. Reagent controlled addition of chiral sulfur ylides to chiral aldehydes. Beilstein Journal of Organic Chemistry. 1: 4. PMID 16542017 DOI: 10.1186/1860-5397-1-4 |
0.449 |
|
| 2005 |
Robiette R, Richardson J, Aggarwal VK, Harvey JN. On the origin of high E selectivity in the Wittig reaction of stabilized ylides: importance of dipole-dipole interactions. Journal of the American Chemical Society. 127: 13468-9. PMID 16190689 DOI: 10.1021/Ja0539589 |
0.726 |
|
| 2005 |
Aggarwal VK, Grange E. Asymmetric sulfonium ylide mediated cyclopropanation: stereocontrolled synthesis of (+)-LY354740. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 568-75. PMID 16187367 DOI: 10.1002/Chem.200500693 |
0.497 |
|
| 2005 |
Aggarwal VK, Harvey JN, Robiette R. On the importance of leaving group ability in reactions of ammonium, oxonium, phosphonium, and sulfonium ylides. Angewandte Chemie (International Ed. in English). 44: 5468-71. PMID 16059960 DOI: 10.1002/Anie.200501526 |
0.734 |
|
| 2005 |
Aggarwal VK, Olofsson B. Enantioselective alpha-arylation of cyclohexanones with diaryl iodonium salts: application to the synthesis of (-)-epibatidine. Angewandte Chemie (International Ed. in English). 44: 5516-9. PMID 16052649 DOI: 10.1002/ANIE.200501745 |
0.713 |
|
| 2005 |
Aggarwal VK, Yu Fang G. Highly regioselective and diastereoselective epoxidation of allylic amines with Oxone. Chemical Communications (Cambridge, England). 3448-50. PMID 15997293 DOI: 10.1039/B503516C |
0.391 |
|
| 2005 |
Aggarwal VK, Patin A, Tisserand S. Highly diastereoselective Diels-Alder reactions of Baylis-Hillman adducts. Organic Letters. 7: 2555-7. PMID 15957889 DOI: 10.1021/Ol050584F |
0.444 |
|
| 2005 |
Aggarwal VK, Hebach C. Carboxylate-stabilised sulfur ylides (thetin salts) in asymmetric epoxidation for the synthesis of glycidic acids. Mechanism and implications. Organic & Biomolecular Chemistry. 3: 1419-27. PMID 15827637 DOI: 10.1039/B418740G |
0.557 |
|
| 2005 |
Aggarwal VK, Fang GY, Schmidt AT. Synthesis and applications of chiral organoboranes generated from sulfonium ylides. Journal of the American Chemical Society. 127: 1642-3. PMID 15700990 DOI: 10.1021/Ja043632K |
0.483 |
|
| 2005 |
Aggarwal VK, Fulford SY, Lloyd-Jones GC. Reevaluation of the mechanism of the Baylis-Hillman reaction: implications for asymmetric catalysis. Angewandte Chemie (International Ed. in English). 44: 1706-8. PMID 15693043 DOI: 10.1002/Anie.200462462 |
0.404 |
|
| 2005 |
Aggarwal VK, Aragoncillo C, Winn CL. Simple preparation of trans-epoxides via ylide intermediates Synthesis. 1378-1382. DOI: 10.1055/S-2004-834885 |
0.494 |
|
| 2005 |
Aggarwal VK, Astle CJ, Iding H, Wirz B, Rogers-Evans M. Separation of pyrrolidine allylation products by diastereoselective enzymatic ester hydrolysis Tetrahedron Letters. 46: 945-947. DOI: 10.1016/J.Tetlet.2004.12.062 |
0.354 |
|
| 2005 |
Fulton JR, Aggarwal VK, De Vicente J. The use of tosylhydrazone salts as a safe alternative for handling diazo compounds and their applications in organic synthesis European Journal of Organic Chemistry. 1479-1492. DOI: 10.1002/Ejoc.200400700 |
0.472 |
|
| 2004 |
Aggarwal VK, Winn CL. Catalytic, asymmetric sulfur ylide-mediated epoxidation of carbonyl compounds: scope, selectivity, and applications in synthesis. Accounts of Chemical Research. 37: 611-20. PMID 15311960 DOI: 10.1021/Ar030045F |
0.5 |
|
| 2004 |
Aggarwal VK, Astle CJ, Rogers-Evans M. A concise asymmetric route to the bridged bicyclic tropane alkaloid ferruginine using enyne ring-closing metathesis. Organic Letters. 6: 1469-71. PMID 15101769 DOI: 10.1021/Ol049665M |
0.473 |
|
| 2004 |
Aggarwal VK, Charmant J, Dudin L, Porcelloni M, Richardson J. Effect of sulfide structure on enantioselectivity in catalytic asymmetric epoxidation of aldehydes: mechanistic insights and implications. Proceedings of the National Academy of Sciences of the United States of America. 101: 5467-71. PMID 15034181 DOI: 10.1073/Pnas.0307559101 |
0.483 |
|
| 2004 |
Aggarwal VK, Roseblade S, Alexander R. The use of enantiomerically pure ketene dithioacetal bis(sulfoxides) in highly diastereoselective intramolecular nitrone cycloadditions. Application in the total synthesis of the beta-amino acid (-)-cispentacin and the first asymmetric synthesis of cis-(3R,4R)-4-amino-pyrrolidine-3-carboxylic acid. Organic & Biomolecular Chemistry. 1: 684-91. PMID 12929455 |
0.401 |
|
| 2004 |
Aggarwal VK, de Vicente J, Bonnert RV. A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ. The Journal of Organic Chemistry. 68: 5381-3. PMID 12816503 DOI: 10.1021/jo0268409 |
0.304 |
|
| 2004 |
Aggarwal VK, Davies PW, Schmidt AT. Asymmetric synthesis of avenaciolide via cascade palladium catalysed cyclisation-carbonylation of bromodienes Chemical Communications. 10: 1232-1233. DOI: 10.1039/B403183K |
0.533 |
|
| 2004 |
Aggarwal VK, Bae I, Lee HY. Application of sulfur ylide mediated epoxidations in the asymmetric synthesis of β-hydroxy-δ-lactones. Synthesis of a mevinic acid analogue and (+)-prelactone B Tetrahedron. 60: 9725-9733. DOI: 10.1016/J.Tet.2004.07.044 |
0.624 |
|
| 2003 |
Aggarwal VK, Belfield AJ. Catalytic asymmetric Nazarov reactions promoted by chiral Lewis acid complexes. Organic Letters. 5: 5075-8. PMID 14682768 DOI: 10.1021/Ol036133H |
0.44 |
|
| 2003 |
Aggarwal VK, Richardson J. The complexity of catalysis: origins of enantio- and diastereocontrol in sulfur ylide mediated epoxidation reactions. Chemical Communications (Cambridge, England). 2644-51. PMID 14649793 DOI: 10.1039/B304625G |
0.489 |
|
| 2003 |
Adams LA, Aggarwal VK, Bonnert RV, Bressel B, Cox RJ, Shepherd J, De Vicente J, Walter M, Whittingham WG, Winn CL. Diastereoselective Synthesis of Cyclopropane Amino Acids Using Diazo Compounds Generated in Situ Journal of Organic Chemistry. 68: 9433-9440. PMID 14629169 DOI: 10.1021/Jo035060C |
0.437 |
|
| 2003 |
Aggarwal VK, Fang GY, Meek G. Highly diastereoselective Simmons-Smith cyclopropanation of allylic amines. Organic Letters. 5: 4417-20. PMID 14602014 DOI: 10.1021/Ol035713B |
0.453 |
|
| 2003 |
Aggarwal VK, Vasse JL. Asymmetric Sulfur Ylide Mediated Aziridination: Application in the Synthesis of the Side Chain of Taxol Organic Letters. 5: 3987-3990. PMID 14535760 DOI: 10.1021/Ol035554W |
0.474 |
|
| 2003 |
Aggarwal VK, Alonso E, Bae I, Hynd G, Lydon KM, Palmer MJ, Patel M, Porcelloni M, Richardson J, Stenson RA, Studley JR, Vasse JL, Winn CL. A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities. Journal of the American Chemical Society. 125: 10926-40. PMID 12952474 DOI: 10.1021/Ja034606+ |
0.506 |
|
| 2003 |
Aggarwal VK, Grainger RS, Newton GK, Spargo PL, Hobson AD, Adams H. Highly diastereoselective 1,3-dipolar cycloaddition reactions of trans-2-methylene-1,3-dithiolane 1,3-dioxide with 3-oxidopyridinium and 3-oxidopyrylium betaines: A route to the tropane skeleton Organic and Biomolecular Chemistry. 1: 1884-1893. PMID 12945769 DOI: 10.1039/B302834H |
0.499 |
|
| 2003 |
Aggarwal VK, Bae I, Lee HY, Richardson J, Williams DT. Sulfur-ylide-mediated synthesis of functionalized and trisubstituted epoxides with high enantioselectivity; application to the synthesis of CDP-840. Angewandte Chemie (International Ed. in English). 42: 3274-8. PMID 12876742 DOI: 10.1002/Anie.200350968 |
0.612 |
|
| 2003 |
Aggarwal VK, Lopin C, Sandrinelli F. New insights in the mechanism of amine catalyzed epoxidation: dual role of protonated ammonium salts as both phase transfer catalysts and activators of oxone. Journal of the American Chemical Society. 125: 7596-601. PMID 12812501 DOI: 10.1021/ja0289088 |
0.363 |
|
| 2003 |
Aggarwal VK, Fulton JR, Sheldon CG, de Vicente J. Generation of phosphoranes derived from phosphites. A new class of phosphorus ylides leading to high E selectivity with semi-stabilizing groups in Wittig olefinations. Journal of the American Chemical Society. 125: 6034-5. PMID 12785815 DOI: 10.1021/Ja029573X |
0.453 |
|
| 2003 |
Aggarwal VK, Butters M, Davies PW. Palladium catalysed cyclisation-carbonylation of enynes to give cyclic gamma,delta-unsaturated acids. Chemical Communications (Cambridge, England). 1046-7. PMID 12772895 DOI: 10.1039/B300719G |
0.384 |
|
| 2003 |
Aggarwal VK, Steele RM, Ritmaleni R, Barrell JK, Grayson I. Highly enantioselective oxidations of ketene dithioacetals leading to trans bis-sulfoxides. The Journal of Organic Chemistry. 68: 4087-90. PMID 12737597 DOI: 10.1021/Jo034032R |
0.387 |
|
| 2003 |
Aggarwal VK, Fang GY, Charmant JP, Meek G. Tandem formation and [2,3] rearrangement of methylene ammonium ylides derived from amines and the Simmons-Smith reagent. Organic Letters. 5: 1757-60. PMID 12735770 DOI: 10.1021/ol034404i |
0.383 |
|
| 2003 |
Aggarwal VK, Emme I, Fulford SY. Correlation between pK(a) and reactivity of quinuclidine-based catalysts in the Baylis-Hillman reaction: discovery of quinuclidine as optimum catalyst leading to substantial enhancement of scope. The Journal of Organic Chemistry. 68: 692-700. PMID 12558387 DOI: 10.1021/Jo026671S |
0.425 |
|
| 2003 |
Aggarwal VK, Esquivel-Zamora BN. Application of the chiral acyl anion equivalent, trans-1,3-dithiane 1,3-dioxide, to an asymmetric synthesis of (R)-salbutamol. The Journal of Organic Chemistry. 67: 8618-21. PMID 12444646 DOI: 10.1021/Jo026410I |
0.433 |
|
| 2003 |
Aggarwal VK, Roseblade S, Alexander R. The use of enantiomerically pure ketene dithioacetal bis(sulfoxides) in highly diastereoselective intramolecular nitrone cycloadditions. Application in the total synthesis of the β-amino acid (–)-cispentacin and the first asymmetric synthesis of cis-(3R,4R)-4-amino-pyrrolidine-3-carboxylic acid Organic & Biomolecular Chemistry. 1: 684-691. DOI: 10.1039/B212719A |
0.505 |
|
| 2003 |
Aggarwal VK, Lattanzi A, Fuentes D. Ketene Claisen Rearrangement of Camphor-Derived 1,3-Oxathianes: Complete Control of Tertiary and Quaternary Stereogenic Centers. Cheminform. 34. DOI: 10.1039/B206857E |
0.423 |
|
| 2003 |
Aggarwal VK, Belfield AJ. Catalytic Asymmetric Nazarov Reactions Promoted by Chiral Lewis Acid Complexes Organic Letters. 5: 5075-5078. DOI: 10.1021/ol036133h |
0.344 |
|
| 2003 |
Aggarwal VK, Fang GY, Meek G. Highly Diastereoselective Simmons-Smith Cyclopropanation of Allylic Amines Organic Letters. 5: 4417-4420. DOI: 10.1021/ol035713b |
0.447 |
|
| 2003 |
Aggarwal VK, Fang GY, Charmant JPH, Meek G. Tandem formation and [2,3] rearrangement of methylene ammonium ylides derived from amines and the Simmons-Smith reagent Organic Letters. 5: 1757-1760. DOI: 10.1021/Ol034404I |
0.472 |
|
| 2003 |
Aggarwal VK, De Vicente J, Bonnert RV. A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ Journal of Organic Chemistry. 68: 5381-5383. DOI: 10.1021/Jo0268409 |
0.419 |
|
| 2003 |
Aggarwal VK, Lopin C, Sandrinelli F. New insights in the mechanism of amine catalyzed epoxidation: Dual role of protonated ammonium salts as both phase transfer catalysts and activators of Oxone Journal of the American Chemical Society. 125: 7596-7601. DOI: 10.1021/Ja0289088 |
0.462 |
|
| 2003 |
Aggarwal VK, Hynd G, Picoul W, Vasse J. Highly Enantioselective Darzens Reaction of a Camphor-Derived Sulfonium Amide to Give Glycidic Amides and Their Applications in Synthesis. Cheminform. 34. DOI: 10.1002/chin.200305109 |
0.44 |
|
| 2003 |
Aggarwal VK, Richardson J. The complexity of catalysis: Origins of enantio- and diastereocontrol in sulfur ylide mediated epoxidation reactions Chemical Communications. 9: 2644-2651. |
0.304 |
|
| 2002 |
Aggarwal VK, Sheldon CG, Macdonald GJ, Martin WP. A new method for the preparation of silyl enol ethers from carbonyl compounds and (trimethylsilyl)diazomethane in a regiospecific and highly stereoselective manner. Journal of the American Chemical Society. 124: 10300-1. PMID 12197731 DOI: 10.1021/Ja027061C |
0.498 |
|
| 2002 |
Aggarwal VK, Patel M, Studley J. Synthesis of epoxides from aldehydes and tosylhydrazone salts catalysed by triphenylarsine: complete trans selectivity for all combinations of coupling partners. Chemical Communications (Cambridge, England). 1514-5. PMID 12189870 DOI: 10.1039/B204252E |
0.482 |
|
| 2002 |
Aggarwal VK, Hynd G, Picoul W, Vasse JL. Highly enantioselective darzens reaction of a camphor-derived sulfonium amide to give glycidic amides and their applications in synthesis. Journal of the American Chemical Society. 124: 9964-5. PMID 12188641 DOI: 10.1021/Ja0272540 |
0.513 |
|
| 2002 |
Aggarwal VK, Emme I, Mereu A. Unexpected side reactions of imidazolium-based ionic liquids in the base-catalysed Baylis-Hillman reaction. Chemical Communications (Cambridge, England). 1612-3. PMID 12170807 DOI: 10.1039/B203079A |
0.376 |
|
| 2002 |
Aggarwal VK, Davies PW, Moss WO. A palladium catalysed cyclisation-carbonylation of bromodienes: control in carbonylation over facile beta-hydride elimination. Chemical Communications (Cambridge, England). 972-3. PMID 12123074 DOI: 10.1039/B201311H |
0.37 |
|
| 2002 |
Aggarwal VK, Harvey JN, Richardson J. Unraveling the mechanism of epoxide formation from sulfur ylides and aldehydes. Journal of the American Chemical Society. 124: 5747-56. PMID 12010049 DOI: 10.1021/Ja025633N |
0.586 |
|
| 2002 |
Aggarwal VK, Alonso E, Ferrara M, Spey SE. Highly diastereoselective aziridination of imines with trimethylsilyldiazomethane. Subsequent silyl substitution with electrophiles, ring opening, and metalation of C-silylaziridines--a cornucopia of highly selective transformations. The Journal of Organic Chemistry. 67: 2335-44. PMID 11925250 DOI: 10.1021/Jo016312H |
0.46 |
|
| 2002 |
Aggarwal VK, Roseblade SJ, Barrell JK, Alexander R. Highly diastereoselective nitrone cycloaddition onto a chiral ketene equivalent: asymmetric synthesis of cispentacin. Organic Letters. 4: 1227-9. PMID 11922825 DOI: 10.1021/Ol025665F |
0.535 |
|
| 2002 |
Aggarwal VK, Dean DK, Mereu A, Williams R. Rate acceleration of the Baylis-Hillman reaction in polar solvents (water and formamide). Dominant role of hydrogen bonding, not hydrophobic effects, is implicated. The Journal of Organic Chemistry. 67: 510-4. PMID 11798324 DOI: 10.1021/Jo016073Y |
0.422 |
|
| 2002 |
Aggarwal VK, Daly AM. Extension of ring closing metathesis methodology to the synthesis of carbocyclic methyl and silyl enol ethers Chemical Communications. 8: 2490-2491. DOI: 10.1039/B208445G |
0.44 |
|
| 2002 |
Aggarwal VK, Sandrinelli F, Charmant JP. Synthesis of new, highly hindered C2-symmetric trans-(2S,5S)-disubstituted pyrrolidines Tetrahedron: Asymmetry. 13: 87-93. DOI: 10.1016/S0957-4166(02)00032-0 |
0.441 |
|
| 2002 |
Catasús M, Moyano A, Aggarwal VK. Sulphur ylide-mediated stereoselective synthesis of a stable ferrocenyl epoxide Tetrahedron Letters. 43: 3475-3479. DOI: 10.1016/S0040-4039(02)00578-6 |
0.494 |
|
| 2002 |
Aggarwal VK, Castro AM, Mereu A, Adams H. The use of enantiomerically pure N-sulfinimines in asymmetric Baylis–Hillman reactions Tetrahedron Letters. 43: 1577-1581. DOI: 10.1016/S0040-4039(02)00021-7 |
0.442 |
|
| 2002 |
Aggarwal V, Coogan M, Stenson R, Jones R, Fieldhouse R, Blacker J. Developments in the Simmons−Smith-Mediated Epoxidation Reaction European Journal of Organic Chemistry. 2002: 319-326. DOI: 10.1002/1099-0690(20021)2002:2<319::Aid-Ejoc319>3.0.Co;2-R |
0.512 |
|
| 2001 |
Aggarwal VK, Alonso E, Fang G, Ferrara M, Hynd G, Porcelloni M. Application of Chiral Sulfides to Catalytic Asymmetric Aziridination and Cyclopropanation with In Situ Generation of the Diazo Compound. Angewandte Chemie (International Ed. in English). 40: 1433-1436. PMID 29712359 DOI: 10.1002/1521-3773(20010417)40:8<1433::Aid-Anie1433>3.0.Co;2-E |
0.451 |
|
| 2001 |
Aggarwal VK, Alonso E, Hynd G, Lydon KM, Palmer MJ, Porcelloni M, Studley JR. Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with In Situ Generation of Diazocompounds. Angewandte Chemie (International Ed. in English). 40: 1430-1433. PMID 29712341 DOI: 10.1002/1521-3773(20010417)40:8<1430::Aid-Anie1430>3.0.Co;2-W |
0.43 |
|
| 2001 |
Aggarwal VK, de Vicente J, Bonnert RV. Catalytic cyclopropanation of alkenes using diazo compounds generated in situ. A novel route to 2-arylcyclopropylamines. Organic Letters. 3: 2785-8. PMID 11506634 DOI: 10.1021/Ol0164177 |
0.452 |
|
| 2001 |
Aggarwal VK, Charmant JPH, Ciampi C, Hornby JM, O'Brien CJ, Hynd G, Parsons R. Additions of stabilised and semi-stabilised sulfur ylides to tosyl protected imines: are they under kinetic or thermodynamic control? Journal of the Chemical Society-Perkin Transactions 1. 3159-3166. DOI: 10.1039/B107275G |
0.497 |
|
| 2001 |
Aggarwal VK, Angelaud R, Bihan D, Blackburn P, Fieldhouse R, Fonquerna SJ, Ford GD, Hynd G, Jones E, Jones RVH, Jubault P, Palmer MJ, Ratcliffe PD, Adams H. Synthesis and evaluation of a broad range of chiral sulfides for asymmetric sulfur ylide epoxidation of aldehydes Journal of the Chemical Society-Perkin Transactions 1. 2604-2622. DOI: 10.1039/B105416N |
0.504 |
|
| 2001 |
Aggarwal VK, Ferrara M, O'Brien CJ, Thompson A, Jones RVH, Fieldhouse R. Scope and limitations in sulfur ylide mediated catalytic asymmetric aziridination of imines: use of phenyldiazomethane, diazoesters and diazoacetamides Journal of the Chemical Society-Perkin Transactions 1. 1635-1643. DOI: 10.1039/B102578N |
0.628 |
|
| 2001 |
Aggarwal VK, Stenson RA, Jones RVH, Fieldhouse R, Blacker J. A novel procedure for the synthesis of aziridines: Application of Simmons-Smith reagents to aziridination Tetrahedron Letters. 42: 1587-1589. DOI: 10.1016/S0040-4039(00)02310-8 |
0.457 |
|
| 2001 |
Aggarwal VK, Alonso E, Fang G, Ferrara M, Hynd G, Porcelloni M. Verwendung chiraler Sulfide zur katalytischen asymmetrischen Aziridinierung und Cyclopropanierung mit in situ gebildeter Diazokomponente Angewandte Chemie. 113: 1482-1485. DOI: 10.1002/1521-3757(20010417)113:8<1482::Aid-Ange1482>3.0.Co;2-X |
0.366 |
|
| 2000 |
Aggarwal VK, Ferrara M. Highly selective aziridination of imines using trimethylsilyldiazomethane and applications of C-silylaziridines in synthesis Organic Letters. 2: 4107-4110. PMID 11112655 DOI: 10.1021/Ol006772H |
0.478 |
|
| 2000 |
Aggarwal VK, Smith HW, Hynd G, Jones RVH, Fieldhouse R, Spey SE. Catalytic cyclopropanation of electron deficient alkenes mediated by chiral and achiral sulfides: Scope and limitations in reactions involving phenyldiazomethane and ethyl diazoacetate Journal of the Chemical Society, Perkin Transactions 1. 3267-3276. DOI: 10.1039/B004367M |
0.493 |
|
| 2000 |
Aggarwal VK, Eames J, Villa M, McIntyre S, Sansbury FH, Warren S. Stereochemical control in the synthesis of tetrahydrofurans by cyclisation of diols with [1,2]-phenylsulfanyl migration Journal of the Chemical Society-Perkin Transactions 1. 2000: 533-546. DOI: 10.1039/A908810E |
0.566 |
|
| 2000 |
Adamo MFA, Aggarwal VK, Sage MA. Epoxidation of Alkenes by Amine Catalyst Precursors: Implication of Aminium Ion and Radical Cation Intermediates Journal of the American Chemical Society. 122: 8317-8318. DOI: 10.1021/Ja0004433 |
0.341 |
|
| 2000 |
Aggarwal VK, De Vicente J, Pelotier B, Holmes IP, Bonnert RV. A simple, user-friendly process for the homologation of aldehydes using tosylhydrazone salts Tetrahedron Letters. 41: 10327-10331. DOI: 10.1016/S0040-4039(00)01856-6 |
0.468 |
|
| 2000 |
Aggarwal VK, Ford JG, Thompson A, Studley J, Jones RVH, Fieldhouse R. ChemInform Abstract: Sulfur Ylide Mediated Catalytic Asymmetric Epoxidation and Aziridination Cheminform. 31: no-no. DOI: 10.1002/chin.200041236 |
0.617 |
|
| 2000 |
Aggarwal V, Jones D, Martin-Castro A. Copper(II)-Bisoxazoline-Catalysed Asymmetric Diels−Alder Reactions of α-Thioacrylates European Journal of Organic Chemistry. 2000: 2939-2945. DOI: 10.1002/1099-0690(200008)2000:16<2939::Aid-Ejoc2939>3.0.Co;2-K |
0.422 |
|
| 1999 |
Aggarwal VK, Barrell JK, Worrall JM, Alexander R. Diastereomerically Pure SpirocyclicBis-Sulfinyl Oxiranes and their Application to the Asymmetric Synthesis of α-Amino Amides Phosphorus, Sulfur, and Silicon and the Related Elements. 153: 337-338. DOI: 10.1080/10426509908546459 |
0.398 |
|
| 1999 |
Adamo MFA, Aggarwal VK, Sage MA. An Improved Resolution Of 2-Methyl Piperidine And Its Use in The Synthesis Of Homochiral Trans-2,6-Dialkyl Piperidines Synthetic Communications. 29: 1747-1756. DOI: 10.1080/00397919908086162 |
0.437 |
|
| 1999 |
Aggarwal VK, Mereu A. Superior amine catalysts for the Baylis–Hillman reaction: the use of DBU and its implications† Chemical Communications. 1999: 2311-2312. DOI: 10.1039/A907754E |
0.386 |
|
| 1999 |
Aggarwal VK, Bethel PA, Giles R. A formal synthesis of (+)-pyripyropene A using a biomimetic epoxy-olefin cyclisation: effect of epoxy alcohol/ether on cyclisation efficiency Journal of the Chemical Society-Perkin Transactions 1. 1999: 3315-3321. DOI: 10.1039/A906589J |
0.482 |
|
| 1999 |
Aggarwal VK, Humphries PS, Fenwick A. Enantioselective deprotonation of 4-tert-butylcyclohexanone by conformationally constrained chiral lithium amide bases Journal of the Chemical Society-Perkin Transactions 1. 1999: 2883-2889. DOI: 10.1039/A905947D |
0.484 |
|
| 1999 |
Aggarwal VK, Bethel PA, Giles R. A formal synthesis of (+)-pyripyropene A using a biomimetic epoxy-olefin cyclisation Chemical Communications. 1999: 325-326. DOI: 10.1039/A808644C |
0.514 |
|
| 1999 |
Aggarwal VK, Masters SJ, Adams H, Spey SE, Brown GR, Foubister AJ. The effects of different ester and ketal protecting groups on the reactivity and selectivity of tartrate-derived silylketene acetals Journal of the Chemical Society-Perkin Transactions 1. 1999: 155-162. DOI: 10.1039/A807863G |
0.513 |
|
| 1999 |
Aggarwal VK, Ferrara M, Hainz R, Spey SE. [2,3]-Sigmatropic rearrangement of allylic sulfur ylides derived from trimethylsilyldiazomethane (TMSD) Tetrahedron Letters. 40: 8923-8927. DOI: 10.1016/S0040-4039(99)01896-1 |
0.518 |
|
| 1999 |
Aggarwal VK, Ali A, Coogan MP. The development and use of ketene equivalents in [4+2] cycloadditions for organic synthesis Tetrahedron. 55: 293-312. DOI: 10.1016/S0040-4020(98)00924-7 |
0.373 |
|
| 1999 |
Aggarwal VK, Humphries PS, Fenwick A. A Formal Asymmetric Synthesis of (+)-Anatoxin-a Using an Enantioselective Deprotonation Strategy on an Eight-Membered Ring Angewandte Chemie International Edition. 38: 1985-1986. DOI: 10.1002/(Sici)1521-3773(19990712)38:13/14<1985::Aid-Anie1985>3.0.Co;2-7 |
0.537 |
|
| 1998 |
Aggarwal VK, Barrell JK, Worrall JM, Alexander R. Highly Diastereoselective Epoxidation of Ketene Dithioacetal Dioxides: A New Approach to the Asymmetric Synthesis of alpha-Amino Amides. The Journal of Organic Chemistry. 63: 7128-7129. PMID 11672347 DOI: 10.1021/Jo9814896 |
0.381 |
|
| 1998 |
Aggarwal VK, Vennall GP. Sc(OTf)3, an Efficient Catalyst for Addition of Allyltrimethylsilane to Aldehydes; Chemoselective Addition to Aldehydes in Presence of Ketones and in situ Acylation (3 Component Coupling) Synthesis. 1998: 1822-1826. DOI: 10.1055/S-1998-2222 |
0.422 |
|
| 1998 |
Aggarwal VK, Fonquerna S, Vennall GP. Sc(OTf)3, an Efficient Catalyst for Formation and Deprotection of Geminal Diacetates (Acylals); Chemoselective Protection of Aldehydes in Presence of Ketones Synlett. 1998: 849-850. DOI: 10.1055/S-1998-1799 |
0.413 |
|
| 1998 |
Aggarwal VK. Catalytic Asymmetric Epoxidation And Aziridination Mediated By Sulfur Ylides. Evolution Of A Project Synlett. 1998: 329-336. DOI: 10.1055/S-1998-1652 |
0.316 |
|
| 1998 |
Aggarwal VK, Anderson ES, Jones DE, Obierey KB, Giles R. Catalytic asymmetric Diels–Alder reactions of α-thioacrylates for the preparation of norbornenone Chemical Communications. 1998: 1985-1986. DOI: 10.1039/A805366I |
0.463 |
|
| 1998 |
Aggarwal VK, Gültekin Z, Grainger RS, Adams H, Spargo PL. (1R,3R)-2-Methylene-1,3-dithiolane 1,3-dioxide: a highly reactive and highly selective chiral ketene equivalent in cycloaddition reactions with a broad range of dienes Journal of the Chemical Society-Perkin Transactions 1. 1998: 2771-2782. DOI: 10.1039/A804607G |
0.515 |
|
| 1998 |
Aggarwal VK, Bell L, Coogan MP, Jubault P. Bifunctional catalysts for catalytic asymmetric sulfur ylide epoxidation of carbonyl compounds Journal of the Chemical Society-Perkin Transactions 1. 2037-2042. DOI: 10.1039/A802362J |
0.367 |
|
| 1998 |
Aggarwal VK, Grainger RS, Adams H, Spargo PL. 1,3-Dipolar Cycloaddition Reactions oftrans-2-Methylene-1,3-dithiolane 1,3-Dioxide with Nitrones The Journal of Organic Chemistry. 63: 3481-3485. DOI: 10.1021/Jo972052L |
0.557 |
|
| 1998 |
Aggarwal VK, Ford JG, Fonquerna S, Adams H, Jones RVH, Fieldhouse R. Catalytic asymmetric epoxidation of aldehydes. Optimization, mechanism, and discovery of stereoelectronic control involving a combination of anomeric and cieplak effects in sulfur ylide epoxidations with chiral 1,3-oxathianes Journal of the American Chemical Society. 120: 8328-8339. DOI: 10.1021/Ja9812150 |
0.482 |
|
| 1998 |
Aggarwal VK, Ford JG, Jones RVH, Fieldhouse R. Camphor derived 1,4-oxathianes for carbonyl epoxidation Tetrahedron Asymmetry. 9: 1801-1807. DOI: 10.1016/S0957-4166(98)00028-7 |
0.44 |
|
| 1998 |
Aggarwal VK, Blackburn P, Fieldhouse R, Jones RVH. Catalytic sulfur ylide reactions: Use of diazoacetamides for the diastereoselective synthesis of glycidic amides Tetrahedron Letters. 39: 8517-8520. DOI: 10.1016/S0040-4039(98)01852-8 |
0.499 |
|
| 1998 |
Aggarwal V, Vennall G, Davey P, Newman C. Scandium trifluoromethaneslfonate, an efficient catalyst for the intermolecular carbonyl-ene reaction and the intramolecular cyclisation of citronellal Tetrahedron Letters. 39: 1997-2000. DOI: 10.1016/S0040-4039(98)00115-4 |
0.427 |
|
| 1997 |
Aggarwal VK, Thompson A, Jones RV, Standen MC. Catalytic and Asymmetric Aziridination using Sulfur Ylides. Phosphorus, Sulfur, and Silicon and the Related Elements. 120: 361-362. DOI: 10.1080/10426509708545549 |
0.638 |
|
| 1997 |
Aggarwal VK, Worrall JM, Alexander R. Stereoselective Epoxidation of bis-Sulfinyl Alkenes and Application to the Asymmetric Synthesis of α-Substituted Carboxylic Acids Phosphorus, Sulfur, and Silicon and the Related Elements. 120: 351-352. DOI: 10.1080/10426509708545544 |
0.453 |
|
| 1997 |
Aggarwal VK, Smith HW, Jones RVH, Fieldhouse R. Catalytic Asymmetric Cyclopropanation Of Electron Deficient Alkenes Mediated By Chiral Sulfides Chemical Communications. 1785-1786. DOI: 10.1039/A704214K |
0.404 |
|
| 1997 |
Aggarwal VK, Monteiro N. Asymmetric total synthesis of (+)-carbocyclic uracil polyoxin C Journal of the Chemical Society-Perkin Transactions 1. 2531-2538. DOI: 10.1039/A702323E |
0.539 |
|
| 1997 |
Aggarwal VK, Calamai S, Ford JG. Additions of benzylsulfonium ylides to aldehydes and ketones: are they under kinetic or thermodynamic control? Journal of the Chemical Society-Perkin Transactions 1. 593-600. DOI: 10.1039/A606925H |
0.501 |
|
| 1997 |
Aggarwal VK, Boccardo G, Worrall JM, Adams H, Alexander R. 2-Halogeno-1,3-dithiane 1,3-dioxide: a diastereoselective carbonyl anionequivalent in reactions with aldehydes Journal of the Chemical Society-Perkin Transactions 1. 11-20. DOI: 10.1039/A603416K |
0.512 |
|
| 1997 |
Aggarwal VK, Ali A, Coogan MP. A Novel Procedure for the Synthesis of Epoxides: Application of Simmons−Smith Reagents toward Epoxidation The Journal of Organic Chemistry. 62: 8628-8629. DOI: 10.1021/Jo971773H |
0.417 |
|
| 1997 |
Aggarwal VK, Monteiro N, Tarver GJ, McCague R. Scope and Limitations in Palladium-Catalyzed Substitution Reactions of Unsaturated Fused Lactones The Journal of Organic Chemistry. 62: 4665-4671. DOI: 10.1021/Jo962106B |
0.478 |
|
| 1997 |
Aggarwal VK, Schade S, Adams H. Anion Reactions oftrans-1,3-Dithiolane 1,3-Dioxide with Aldehydes and Comparison withtrans-1,3-Dithiane 1,3-Dioxide The Journal of Organic Chemistry. 62: 1139-1145. DOI: 10.1021/Jo9619443 |
0.414 |
|
| 1997 |
Aggarwal VK, Vennall GP, Davey PN, Newman C. Trifluoromethanesulfonic Acid, an Efficient Catalyst for the Hetero Diels-Alder Reaction and an Improved Synthesis of Mefrosol. Tetrahedron Letters. 38: 2569-2572. DOI: 10.1016/S0040-4039(97)00403-6 |
0.455 |
|
| 1997 |
Aggarwal VK, Thomas A, Schade S. trans-1,3-dithiane-1,3-dioxide; a chiral acyl anion equivalent. Enantioselective synthesis of α-hydroxy- carboxylic acids, esters, amides and ketones Tetrahedron. 53: 16213-16228. DOI: 10.1016/S0040-4020(97)01010-7 |
0.483 |
|
| 1996 |
Aggarwal VK, Tarver GJ, McCague R. First examples of metal and ligand accelerated catalysis of the Baylis–Hillman reaction Chemical Communications. 2713-2714. DOI: 10.1039/Cc9960002713 |
0.405 |
|
| 1996 |
Aggarwal VK, Wang MF. Catalytic asymmetric synthesis of epoxides mediated by chiral iminium salts Chemical Communications. 191-192. DOI: 10.1039/Cc9960000191 |
0.442 |
|
| 1996 |
Aggarwal VK, Eames J, Heras MAdl, McIntyre S, Warren S. Scope and limitation of the [1,4] SPh shift in the synthesis of allylic alcohols Journal of the Chemical Society-Perkin Transactions 1. 37: 4456-4461. DOI: 10.1039/B005349J |
0.414 |
|
| 1996 |
Aggarwal VK, Thompson A, Jones RVH, Standen MCH. Novel Catalytic and Asymmetric Process for Aziridination Mediated by Sulfur Ylides The Journal of Organic Chemistry. 61: 8368-8369. DOI: 10.1021/Jo961754S |
0.609 |
|
| 1996 |
Aggarwal VK, Monteiro N, Tarver GJ, Lindell SD. Palladium-Catalyzed Substitution of Unsaturated Lactones. Application to the Synthesis of Carbocyclic Polyoxins and Nikkomycins The Journal of Organic Chemistry. 61: 1192-1193. DOI: 10.1021/Jo952187W |
0.537 |
|
| 1996 |
Aggarwal VK, Ford JG, Thompson A, Jones RVH, Standen MCH. Direct Asymmetric Epoxidation of Aldehydes Using Catalytic Amounts of Enantiomerically Pure Sulfides Journal of the American Chemical Society. 118: 7004-7005. DOI: 10.1021/Ja961144+ |
0.67 |
|
| 1996 |
Aggarwal VK, Jones D, Turner ML, Adams H. First synthesis and X-ray crystal structure of 1,2-(1,1′-ferrocenediyl)ethene Journal of Organometallic Chemistry. 524: 263-266. DOI: 10.1016/S0022-328X(96)06330-9 |
0.352 |
|
| 1996 |
Aggarwal V, Vennall G. Scandium trifluoromethanesulfonate, a novel catalyst for the addition of allyltrimethylsilane to aldehydes Tetrahedron Letters. 37: 3745-3746. DOI: 10.1016/0040-4039(96)00636-3 |
0.367 |
|
| 1996 |
Aggarwal VK, Abdel-Rahman H, Fan L, Jones RVH, Standen MCH. A Novel Catalytic Cycle for the Synthesis of Epoxides Using Sulfur Ylides Chemistry - a European Journal. 2: 1024-1030. DOI: 10.1002/Chem.19960020819 |
0.456 |
|
| 1995 |
Aggarwal VK, Franklin R, Maddock J, Evans GR, Thomas A, Mahon MF, Molloy KC, Rice MJ. Anion Reactions of 1,3-Dithiane 1,3-Dioxide with Carbonyl Compounds: High Diastereoselectivity with Aromatic Aldehydes under Conditions of Equilibrium Control The Journal of Organic Chemistry. 60: 2174-2182. DOI: 10.1021/Jo00112A042 |
0.425 |
|
| 1995 |
Aggarwal VK, Thompson A, Jones RV, Standen M. The use of chiral sulfides in catalytic asymmetric epoxidation Tetrahedron: Asymmetry. 6: 2557-2564. DOI: 10.1016/0957-4166(95)00334-L |
0.665 |
|
| 1995 |
Aggarwal VK, Anderson E, Giles R, Zaparucha A. Complexes containing a Lewis acid and Brønsted acid for the catalytic asymmetric Diels-Alder reaction Tetrahedron: Asymmetry. 6: 1301-1306. DOI: 10.1016/0957-4166(95)00163-J |
0.397 |
|
| 1995 |
Aggarwal VK, Abdel-Rahman H, Jones RV, Standen MC. A novel catalytic cycle for the synthesis-of epoxides using sulfur ylides: Application to base sensitive aldehydes Tetrahedron Letters. 36: 1731-1732. DOI: 10.1016/0040-4039(95)00103-J |
0.456 |
|
| 1995 |
AGGARWAL VK, THOMPSON A, JONES RVH. ChemInform Abstract: Synthesis of Sulfonium Salts by Sulfide Alkylation; an Alternative Approach. Cheminform. 26: no-no. DOI: 10.1002/chin.199516079 |
0.613 |
|
| 1994 |
Aggarwal VK, Grainger RS, Spargo PL. Asymmetric Synthesis and Cycloaddition Chemistry of Trans-2-Methylene-1,3-Dithiolane 1,3-Dioxide Phosphorus, Sulfur, and Silicon and the Related Elements. 95: 337-338. DOI: 10.1080/10426509408034227 |
0.549 |
|
| 1994 |
Aggarwal VK, Abdel-rahman H, Thompson A, Mattison B, Jones RVH. A Novel Catalytic Cycle for the Synthesis of Epoxides Using Sulfur Ylides, and Application to the Synthesis of Cyclopropanes and Aziridines Phosphorus, Sulfur, and Silicon and the Related Elements. 95: 283-292. DOI: 10.1080/10426509408034213 |
0.703 |
|
| 1994 |
Aggarwal VK, Thomas A, Franklin RJ. trans-1,3-Dithiane-1,3-dioxide, a new chiral acyl anion equivalent for the preparation of masked activated acids: application to the synthesis of α-hydroxy acid derivatives Journal of the Chemical Society, Chemical Communications. 1653-1654. DOI: 10.1039/C39940001653 |
0.5 |
|
| 1994 |
Aggarwal VK, Wang MF, Zaparucha A. The first synthesis of the novel 2,8-dioxabicyclo[3.2.1]octane ring system: a key feature of the squalestatins Journal of the Chemical Society, Chemical Communications. 87-88. DOI: 10.1039/C39940000087 |
0.448 |
|
| 1994 |
Aggarwal VK, Abdel-Rahman H, Jones RVH, Lee HY, Reid BD. Novel Catalytic Cycle for the Synthesis of Epoxides from Aldehydes and Sulfur Ylides Mediated by Catalytic Quantities of Sulfides and Rh2(OAc)4 Journal of the American Chemical Society. 116: 5973-5974. DOI: 10.1021/Ja00092A060 |
0.48 |
|
| 1994 |
Aggarwal VK, Thompson A, Jones RV. Synthesis of sulfonium salts by sulfide alkylation; an alternative approach Tetrahedron Letters. 35: 8659-8660. DOI: 10.1016/S0040-4039(00)78464-4 |
0.68 |
|
| 1994 |
Aggarwal VK, Kalomiri M, Thomas AP. Asymmetric epoxidation using chiral sulfur ylides Tetrahedron: Asymmetry. 5: 723-730. DOI: 10.1016/0957-4166(94)80035-9 |
0.498 |
|
| 1994 |
Aggarwal VK, Worrall JM, Adams H, Alexander R. Stereoselective addition reactions of lithiated 2-chloro-1,3-dithiane-1,3-dioxide to aldehydes Tetrahedron Letters. 35: 6167-6170. DOI: 10.1016/0040-4039(94)88106-5 |
0.457 |
|
| 1994 |
Aggarwal VK. Enantioselective Transformations and Racemization Studies of Heteroatom Substituted Organolithium Compounds Angewandte Chemie International Edition in English. 33: 175-177. DOI: 10.1002/Anie.199401751 |
0.342 |
|
| 1993 |
Aggarwal VK, Lightowler M. Chiral Ketene Equivalents for Use in Asymmetric Synthesis Phosphorus, Sulfur, and Silicon and the Related Elements. 74: 407-408. DOI: 10.1080/10426509308038138 |
0.462 |
|
| 1992 |
Aggarwal VK, Lightowler M, Lindell SD. trans-Dioxides of Cyclic Ketene Thioacetals: Highly Selective Chiral Ketene Equivalents Synlett. 1992: 730-732. DOI: 10.1055/S-1992-21471 |
0.396 |
|
| 1992 |
Aggarwal VK, Evans G, Moya E, Dowden J. Chiral bisfunctionalization of substrates: a powerful strategy for the asymmetric synthesis of C2 symmetric compounds and its application to the synthesis of enantiomerically pure trans-1,3-dithiane 1,3-dioxide Journal of Organic Chemistry. 57: 6390-6391. DOI: 10.1021/Jo00050A008 |
0.418 |
|
| 1991 |
Aggarwal VK, Davies IW, Franklin RJ, Maddock J, Mahon MF, Molloy KC. Synthesis, X-ray crystal structure, equilibration studies and anion chemistry of trans-1,3-dithiane 1,3-dioxide Journal of the Chemical Society-Perkin Transactions 1. 662-664. DOI: 10.1039/P19910000662 |
0.4 |
|
| 1991 |
Aggarwal VK, Coldham I, McIntyre S, Warren S. Transformation of cyclic α-phenylthio aldehydes by stereoselective aldol reactions and phenylthio migration into spirocyclic lactones and ethers, and E-allylic alcohols with 1,4-related chiral centres Journal of the Chemical Society-Perkin Transactions 1. 451-460. DOI: 10.1039/P19910000451 |
0.609 |
|
| 1991 |
Aggarwal VK, Franklin RJ, Rice MJ. Highly stereoselective addition reactions of metallated trans-1,3-dithiane-1,3-dioxide to aldehydes Tetrahedron Letters. 32: 7743-7746. DOI: 10.1016/0040-4039(91)80580-Y |
0.482 |
|
| 1990 |
Aggarwal VK, Davies IW, Maddock J, Mahon MF, Molloy KC. Additions of aldehydes to metallated trans-1,3-Dithiane-S,S-dioxide under conditions of kinetic and thermodynamic control Tetrahedron Letters. 31: 135-138. DOI: 10.1016/S0040-4039(00)94354-5 |
0.427 |
|
| 1988 |
Aggarwal VK, Coldham I, McIntyre S, Sansbury FH, Villa M, Warren S. Stereochemical control in the synthesis of tetrahydrofurans by cyclisation of diols with phenylthio migration Tetrahedron Letters. 29: 4885-4888. DOI: 10.1016/S0040-4039(00)80634-6 |
0.509 |
|
| 1988 |
AGGARWAL VK, WARREN S. ChemInform Abstract: Allyl Sulfide Synthesis of Phenylthio Migration: Relationship Between Stereochemistry of Starting Materials and Regioselectivity of Double Bond Formation. Cheminform. 19. DOI: 10.1002/chin.198813162 |
0.313 |
|
| 1987 |
Aggarwal VK, Warren S. Allyl sulphide synthesis by phenylthio migration: relationship between stereochemistry of starting materials and regioselectivity of double bond formation Journal of the Chemical Society-Perkin Transactions 1. 2579-2584. DOI: 10.1039/P19870002579 |
0.571 |
|
| 1987 |
Aggarwal VK, Warren S. Synthesis of compounds with 1,4-related chiral centres by phenylthio migration: and --2,4-dimethylhex-3-ene-1,5-diol Tetrahedron Letters. 28: 1925-1928. DOI: 10.1016/S0040-4039(00)96011-8 |
0.533 |
|
| 1986 |
Aggarwal VK, Warren S. Phenylthio(Phs) migration in the stereocontrolled synthesis of allylic alcohols with 1, 4 related chiral centres. Tetrahedron Letters. 27: 101-104. DOI: 10.1016/S0040-4039(00)83952-0 |
0.541 |
|
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