| Year |
Citation |
Score |
| 2023 |
Crompton JL, Frost JR, Rowe SM, Christensen KE, Donohoe TJ. Synthesis of Cyclopropanes via Hydrogen-Borrowing Catalysis. Organic Letters. PMID 37428545 DOI: 10.1021/acs.orglett.3c01768 |
0.385 |
|
| 2023 |
Smith L, Armstrong R, Hou J, Smith E, Sze M, Sterling A, Smith A, Duarte F, Donohoe TJ. Redox Reorganization: Aluminium Promoted 1,5-Hydride Shifts Allow the Controlled Synthesis of Multisubstituted Cyclohexenes. Angewandte Chemie (International Ed. in English). e202307424. PMID 37358307 DOI: 10.1002/anie.202307424 |
0.359 |
|
| 2023 |
Day AJ, Jenkins TC, Kischkewitz M, Christensen KE, Poole DL, Donohoe TJ. Metal and Activating Group Free C-4 Alkylation of Isoquinolines via a Temporary Dearomatization Strategy. Organic Letters. 25: 614-618. PMID 36688518 DOI: 10.1021/acs.orglett.2c04149 |
0.324 |
|
| 2022 |
Kratena N, Marinic B, Donohoe TJ. Recent advances in the dearomative functionalisation of heteroarenes. Chemical Science. 13: 14213-14225. PMID 36545133 DOI: 10.1039/d2sc04638e |
0.343 |
|
| 2022 |
Aynetdinova D, Jacques R, Christensen K, Donohoe TJ. Alcohols as efficient intermolecular initiators for a highly stereoselective polyene cyclisation cascade. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 36478469 DOI: 10.1002/chem.202203732 |
0.349 |
|
| 2022 |
Hoff O, Kratena N, Aynetdinova D, Christensen KE, Donohoe TJ. A Vicinal Diol Approach for the Total Synthesis of Molestin E, ent-Sinulacembranolide A and ent-Sinumaximol A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35946550 DOI: 10.1002/chem.202202464 |
0.369 |
|
| 2022 |
Cox L, Zhu Y, Smith P, Christensen K, Sidera Portela M, Donohoe TJ. Alcohols as Alkylating Agents in the Cation Induced Formation of Nitrogen Heterocycles. Angewandte Chemie (International Ed. in English). PMID 35770710 DOI: 10.1002/anie.202206800 |
0.383 |
|
| 2022 |
Kischkewitz M, Marinic B, Kratena N, Lai Y, Hepburn HB, Dow M, Christensen KE, Donohoe TJ. Evolution of the Dearomative Functionalization of Activated Quinolines and Isoquinolines: Expansion of the Electrophile Scope. Angewandte Chemie (International Ed. in English). e202204682. PMID 35560761 DOI: 10.1002/anie.202204682 |
0.401 |
|
| 2022 |
Hall CJJ, Marriott IS, Christensen KE, Day AJ, Goundry WRF, Donohoe TJ. Extension of hydrogen borrowing alkylation reactions for the total synthesis of (-)-γ-lycorane. Chemical Communications (Cambridge, England). PMID 35348143 DOI: 10.1039/d2cc01248k |
0.4 |
|
| 2021 |
Haughey MB, Christensen KE, Poole DL, Donohoe TJ. Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products. Chemical Science. 12: 13392-13397. PMID 34777757 DOI: 10.1039/d1sc04247e |
0.405 |
|
| 2021 |
Hall CJJ, Goundry WRF, Donohoe TJ. Hydrogen Borrowing Alkylation of 1,2-Amino Alcohols in the Synthesis of Enantioenriched γ-Aminobutyric Acids. Angewandte Chemie (International Ed. in English). PMID 33561302 DOI: 10.1002/anie.202100922 |
0.327 |
|
| 2020 |
Marinic B, Hepburn HB, Grozavu A, Dow M, Donohoe TJ. Single point activation of pyridines enables reductive hydroxymethylation. Chemical Science. 12: 742-746. PMID 34163807 DOI: 10.1039/d0sc05656a |
0.334 |
|
| 2020 |
Grozavu A, Hepburn HB, Bailey EP, Lindsay-Scott PJ, Donohoe TJ. Rhodium catalysed C-3/5 methylation of pyridines using temporary dearomatisation. Chemical Science. 11: 8595-8599. PMID 34123119 DOI: 10.1039/d0sc02759f |
0.331 |
|
| 2020 |
Wubbolt S, Cheong CB, Frost J, Christensen K, Donohoe TJ. A Vinyl Cyclopropane Ring Expansion and Iridium-catalyzed Hydrogen Borrowing Cascade. Angewandte Chemie (International Ed. in English). PMID 32314851 DOI: 10.1002/Anie.202003614 |
0.535 |
|
| 2020 |
Kwok T, Hoff O, Armstrong RJ, Donohoe TJ. Control of Absolute Stereochemistry in Transition-Metal-Catalyzed Hydrogen Borrowing Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32297370 DOI: 10.1002/Chem.202001253 |
0.433 |
|
| 2020 |
Cheang DMJ, Armstrong RJ, Akhtar WM, Donohoe TJ. Enantioconvergent alkylation of ketones with racemic secondary alcohols via hydrogen borrowing catalysis. Chemical Communications (Cambridge, England). PMID 32104853 DOI: 10.1039/D0Cc00767F |
0.437 |
|
| 2020 |
Chamberlain AER, Paterson KJ, Armstrong RJ, Twin HC, Donohoe TJ. A hydrogen borrowing annulation strategy for the stereocontrolled synthesis of saturated aza-heterocycles. Chemical Communications (Cambridge, England). PMID 32104845 DOI: 10.1039/D0Cc00903B |
0.457 |
|
| 2020 |
Smith LB, Armstrong RJ, Matheau-Raven D, Donohoe TJ. Chemo- and Regioselective Synthesis of Acyl-Cyclohexenes by a Tandem Acceptorless Dehydrogenation-[1,5]-Hydride Shift Cascade. Journal of the American Chemical Society. PMID 31967814 DOI: 10.1021/Jacs.9B12296 |
0.493 |
|
| 2020 |
Hepburn HB, Donohoe TJ. Reductive Hydroxymethylation of 4-Heteroarylpyridines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31917881 DOI: 10.1002/Chem.202000060 |
0.401 |
|
| 2020 |
Grozavu A, Hepburn HB, Bailey EP, Lindsay-Scott PJ, Donohoe TJ. Rhodium catalysed C-3/5 methylation of pyridines using temporary dearomatisation Chemical Science. 11: 8595-8599. DOI: 10.1039/D0Sc02759F |
0.44 |
|
| 2020 |
Kelly A, Hoffman JB, Hoff O, Walker JCL, Werrel S, Donohoe TJ. A Heck reaction/photochemical alkene isomerization sequence to prepare functionalized quinolines Tetrahedron. 76: 131396. DOI: 10.1016/J.Tet.2020.131396 |
0.423 |
|
| 2019 |
Reeves BM, Hepburn HB, Grozavu A, Lindsay-Scott PJ, Donohoe TJ. Transition-Metal-Free Reductive Hydroxymethylation of Isoquinolines. Angewandte Chemie (International Ed. in English). PMID 31486205 DOI: 10.1002/Anie.201908857 |
0.383 |
|
| 2019 |
Zhu Y, Colomer I, Donohoe TJ. Hypervalent iodine initiated intramolecular alkene dimerisation: a stereodivergent entry to cyclobutanes. Chemical Communications (Cambridge, England). 55: 10316-10319. PMID 31402367 DOI: 10.1039/C9Cc04383G |
0.421 |
|
| 2019 |
Walker J, Werrel S, Donohoe TJ. Photochemical Alkene Isomerization for the Synthesis of Polysubstituted Furans and Pyrroles under Neutral Conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31390097 DOI: 10.1002/Chem.201903590 |
0.473 |
|
| 2019 |
Richardson MSW, Tame CJ, Poole DL, Donohoe TJ. Rhodium-catalysed vinyl 1,4-conjugate addition coupled with Sharpless asymmetric dihydroxylation in the synthesis of the CDE ring fragment of pectenotoxin-4. Chemical Science. 10: 6336-6340. PMID 31341588 DOI: 10.1039/C9Sc01761E |
0.514 |
|
| 2019 |
Armstrong R, Akhtar W, Young T, Duarte F, Donohoe TJ. Catalytic Asymmetric Synthesis of Cyclohexanes by Hydrogen Borrowing Annulations. Angewandte Chemie (International Ed. in English). PMID 31265208 DOI: 10.1002/Anie.201907514 |
0.469 |
|
| 2019 |
Shirley HJ, Koyioni M, Muncan F, Donohoe TJ. Synthesis of lamellarin alkaloids using orthoester-masked α-keto acids. Chemical Science. 10: 4334-4338. PMID 31057760 DOI: 10.1039/C8Sc05678A |
0.438 |
|
| 2019 |
Zhu Y, Colomer I, Thompson AL, Donohoe TJ. HFIP Solvent Enables Alcohols To Act as Alkylating Agents in Stereoselective Heterocyclization. Journal of the American Chemical Society. PMID 30977361 DOI: 10.1021/Jacs.9B02198 |
0.44 |
|
| 2019 |
Armstrong RJ, Akhtar WM, Frost JR, Christensen KE, Stevenson NG, Donohoe TJ. Stereoselective synthesis of alicyclic ketones: A hydrogen borrowing approach Tetrahedron. 75: 130680. DOI: 10.1016/J.Tet.2019.130680 |
0.527 |
|
| 2018 |
Grozavu A, Hepburn HB, Smith PJ, Potukuchi HK, Lindsay-Scott PJ, Donohoe TJ. The reductive C3 functionalization of pyridinium and quinolinium salts through iridium-catalysed interrupted transfer hydrogenation. Nature Chemistry. PMID 30559370 DOI: 10.1038/S41557-018-0178-5 |
0.461 |
|
| 2018 |
Akhtar WM, Armstrong RJ, Frost JR, Stevenson NG, Donohoe TJ. Stereoselective Synthesis of Cyclohexanes via an Iridium Catalyzed (5 + 1) Annulation Strategy. Journal of the American Chemical Society. PMID 30212192 DOI: 10.1021/Jacs.8B07776 |
0.525 |
|
| 2018 |
Alves Esteves CH, Koyioni M, Christensen KE, Smith PD, Donohoe TJ. OBO-Protected Pyruvates as Reagents for the Synthesis of Functionalized Heteroaromatic Compounds. Organic Letters. PMID 29906124 DOI: 10.1021/Acs.Orglett.8B01614 |
0.452 |
|
| 2018 |
Balcells S, Haughey MB, Walker JCL, Josa-Culleré L, Towers C, Donohoe TJ. Asymmetric Total Synthesis of (-)-(3 R)-Inthomycin C. Organic Letters. PMID 29863350 DOI: 10.1021/Acs.Orglett.8B01370 |
0.44 |
|
| 2017 |
Roushanbakhti A, Liu Y, Winship P, Tucker M, Akhtar W, Walter D, Wrigley G, Donohoe TJ. Cobalt versus osmium: control of both trans and cis selectivity in construction of the EFG rings of pectenotoxin 4. Angewandte Chemie (International Ed. in English). PMID 28926175 DOI: 10.1002/Anie.201708278 |
0.481 |
|
| 2017 |
Alves Esteves CH, Hall CJJ, Smith PD, Donohoe TJ. Pyruvate Enolate Arylation and Alkylation: OBO Ester Protected Pyruvates as Useful Reagents in Organic Synthesis. Organic Letters. PMID 28920691 DOI: 10.1021/Acs.Orglett.7B02524 |
0.524 |
|
| 2017 |
Alves Esteves CH, Smith PD, Donohoe TJ. Catalytic Enolate Arylation with 3-Bromoindoles Allows the Formation of β-Carbolines. The Journal of Organic Chemistry. PMID 28362489 DOI: 10.1021/Acs.Joc.7B00299 |
0.475 |
|
| 2017 |
Akhtar WM, Cheong CB, Frost JR, Christensen KE, Stevenson NG, Donohoe TJ. Hydrogen Borrowing Catalysis with Secondary Alcohols: A New Route for the Generation of β-Branched Carbonyl Compounds. Journal of the American Chemical Society. PMID 28177613 DOI: 10.1021/Jacs.6B12840 |
0.439 |
|
| 2017 |
Winter C, Pullin RD, Donohoe TJ. Diastereoselective synthesis of the 5-hydroxy-pyrrolidinone amino acid of the microsclerodermins and model studies for an end-game strategy for microsclerodermin B Tetrahedron Letters. 58: 602-605. DOI: 10.1016/J.Tetlet.2016.12.045 |
0.404 |
|
| 2016 |
Colomer I, Barcelos RC, Christensen KE, Donohoe TJ. Orthogonally Protected 1,2-Diols from Electron-Rich Alkenes Using Metal-Free Olefin syn-Dihydroxylation. Organic Letters. 18: 5880-5883. PMID 27934501 DOI: 10.1021/Acs.Orglett.6B02959 |
0.389 |
|
| 2016 |
Melikhova EY, Pullin RD, Winter C, Donohoe TJ. Dehydromicrosclerodermin B and Microsclerodermin J: Total Synthesis and Structural Revision. Angewandte Chemie (International Ed. in English). PMID 27418203 DOI: 10.1002/Anie.201604764 |
0.42 |
|
| 2016 |
Colomer I, Batchelor-McAuley C, Odell B, Donohoe TJ, Compton RG. Hydrogen Bonding to Hexafluoroisopropanol Controls the Oxidative Strength of Hypervalent Iodine Reagents. Journal of the American Chemical Society. PMID 27380523 DOI: 10.1021/Jacs.6B04057 |
0.349 |
|
| 2016 |
Colomer I, Coura Barcelos R, Donohoe TJ. Catalytic Hypervalent Iodine Promoters Lead to Styrene Dimerization and the Formation of Tri- and Tetrasubstituted Cyclobutanes. Angewandte Chemie (International Ed. in English). PMID 26948413 DOI: 10.1002/Anie.201511683 |
0.451 |
|
| 2016 |
Donohoe T, Frost J, Cheong C. Iridium-Catalyzed C4-Alkylation of 2,6-Di-tert-butylphenol by Using Hydrogen-Borrowing Catalysis Synthesis. 49: 910-916. DOI: 10.1055/S-0035-1561439 |
0.486 |
|
| 2016 |
Potukuchi HK, Colomer I, Donohoe TJ. Synthesis of Aromatic Heterocycles Using Ring-Closing Metathesis Advances in Heterocyclic Chemistry. 120: 43-65. DOI: 10.1016/Bs.Aihch.2016.04.006 |
0.506 |
|
| 2015 |
Frost JR, Cheong CB, Akhtar WM, Caputo DF, Stevenson NG, Donohoe TJ. Strategic Application and Transformation of ortho-Disubstituted Phenyl and Cyclopropyl Ketones To Expand the Scope of Hydrogen Borrowing Catalysis. Journal of the American Chemical Society. PMID 26654947 DOI: 10.1021/Jacs.5B11196 |
0.518 |
|
| 2015 |
Pilgrim BS, Gatland AE, Esteves CH, McTernan CT, Jones GR, Tatton MR, Procopiou PA, Donohoe TJ. Palladium-catalyzed enolate arylation as a key C-C bond-forming reaction for the synthesis of isoquinolines. Organic & Biomolecular Chemistry. PMID 26632484 DOI: 10.1039/C5Ob02320C |
0.486 |
|
| 2015 |
Spork AP, Donohoe TJ. Aziridine electrophiles in the functionalisation of peptide chains with amine nucleophiles. Organic & Biomolecular Chemistry. 13: 8545-9. PMID 26166551 DOI: 10.1039/C5Ob00856E |
0.373 |
|
| 2015 |
Hardegger LA, Habegger J, Donohoe TJ. Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation. Organic Letters. PMID 26087079 DOI: 10.1021/Acs.Orglett.5B01312 |
0.506 |
|
| 2015 |
Potukuchi HK, Spork AP, Donohoe TJ. Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles. Organic & Biomolecular Chemistry. 13: 4367-73. PMID 25789887 DOI: 10.1039/C5Ob00055F |
0.494 |
|
| 2015 |
Shen D, Poole DL, Shotton CC, Kornahrens AF, Healy MP, Donohoe TJ. Hydrogen-borrowing and interrupted-hydrogen-borrowing reactions of ketones and methanol catalyzed by iridium. Angewandte Chemie (International Ed. in English). 54: 1642-5. PMID 25491653 DOI: 10.1002/Anie.201410391 |
0.432 |
|
| 2015 |
Werrel S, Walker JCL, Donohoe TJ. Application of catalytic Z-selective olefin metathesis in natural product synthesis Tetrahedron Letters. 56: 5261-5268. DOI: 10.1016/J.Tetlet.2015.07.008 |
0.411 |
|
| 2014 |
Gatland AE, Pilgrim BS, Procopiou PA, Donohoe TJ. Short and efficient syntheses of protoberberine alkaloids using palladium-catalyzed enolate arylation. Angewandte Chemie (International Ed. in English). 53: 14555-8. PMID 25348493 DOI: 10.1002/Anie.201409164 |
0.55 |
|
| 2014 |
Tatton MR, Simpson I, Donohoe TJ. New methods for the synthesis of naphthyl amines; application to the synthesis of dihydrosanguinarine, sanguinarine, oxysanguinarine and (±)-maclekarpines B and C. Chemical Communications (Cambridge, England). 50: 11314-6. PMID 25116797 DOI: 10.1039/C4Cc05209A |
0.435 |
|
| 2014 |
Tatton MR, Simpson I, Donohoe TJ. De novo synthesis of multisubstituted aryl amines using alkene cross metathesis. Organic Letters. 16: 1920-3. PMID 24646289 DOI: 10.1021/Ol500441Q |
0.511 |
|
| 2014 |
Chan LK, Poole DL, Shen D, Healy MP, Donohoe TJ. Rhodium-catalyzed ketone methylation using methanol under mild conditions: formation of α-branched products. Angewandte Chemie (International Ed. in English). 53: 761-5. PMID 24288297 DOI: 10.1002/Anie.201307950 |
0.445 |
|
| 2014 |
Donohoe TJ, Jones CR, Winter C. Partial and Complete Reduction of Pyrroles, Furans, Thiophenes, and their Benzo Analogs, Heterocycles Containing More Than One Heteroatom Comprehensive Organic Synthesis: Second Edition. 8: 794-837. DOI: 10.1016/B978-0-08-097742-3.00824-7 |
0.339 |
|
| 2014 |
Chan LKM, Poole DL, Shen D, Healy MP, Donohoe TJ. Back Cover: Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products (Angew. Chem. Int. Ed. 3/2014) Angewandte Chemie International Edition. 53: 892-892. DOI: 10.1002/Anie.201310758 |
0.379 |
|
| 2014 |
Chan LKM, Poole DL, Shen D, Healy MP, Donohoe TJ. Rücktitelbild: Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products (Angew. Chem. 3/2014) Angewandte Chemie. 126: 908-908. DOI: 10.1002/Ange.201310758 |
0.382 |
|
| 2013 |
Donohoe TJ, Jones CR, Kornahrens AF, Barbosa LC, Walport LJ, Tatton MR, O'Hagan M, Rathi AH, Baker DB. Total synthesis of the antitumor antibiotic (±)-streptonigrin: first- and second-generation routes for de novo pyridine formation using ring-closing metathesis. The Journal of Organic Chemistry. 78: 12338-50. PMID 24328139 DOI: 10.1021/Jo402388F |
0.647 |
|
| 2013 |
Pilgrim BS, Gatland AE, McTernan CT, Procopiou PA, Donohoe TJ. Modular isoquinoline synthesis using catalytic enolate arylation and in situ functionalization. Organic Letters. 15: 6190-3. PMID 24251885 DOI: 10.1021/Ol4030309 |
0.525 |
|
| 2013 |
Pullin RD, Rathi AH, Melikhova EY, Winter C, Thompson AL, Donohoe TJ. Tethered aminohydroxylation: synthesis of the β-amino acid of microsclerodermins A and B. Organic Letters. 15: 5492-5. PMID 24131375 DOI: 10.1021/Ol402638N |
0.414 |
|
| 2013 |
Pilgrim BS, Donohoe TJ. Osmium-catalyzed oxidative cyclization of dienes and their derivatives. The Journal of Organic Chemistry. 78: 2149-67. PMID 23369062 DOI: 10.1021/Jo302719Y |
0.482 |
|
| 2013 |
Donohoe TJ, Lipi?ski RM. Interplay of cascade oxidative cyclization and hydride shifts in the synthesis of the ABC spiroketal ring system of pectenotoxin-4. Angewandte Chemie (International Ed. in English). 52: 2491-4. PMID 23362216 DOI: 10.1002/Anie.201208919 |
0.489 |
|
| 2013 |
Pullin RDC, Lipi?ski RM, Donohoe TJ. Oxidative cyclization for the synthesis of complex tetrahydrofuran-containing natural products Pure and Applied Chemistry. 85: 1175-1184. DOI: 10.1351/Pac-Con-12-10-25 |
0.447 |
|
| 2013 |
Baker DB, Gallagher PT, Donohoe TJ. Vinyl Weinreb amides: A versatile alternative to vinyl ketone substrates for the Heck arylation Tetrahedron. 69: 3690-3697. DOI: 10.1016/J.Tet.2013.03.009 |
0.515 |
|
| 2012 |
Donohoe TJ, Pullin RD. Natural product synthesis as a challenging test of newly developed methodology. Chemical Communications (Cambridge, England). 48: 11924-38. PMID 23086503 DOI: 10.1039/C2Cc36040C |
0.347 |
|
| 2012 |
Donohoe TJ, O'Riordan TJ, Peifer M, Jones CR, Miles TJ. Asymmetric synthesis of the fully elaborated pyrrolidinone core of oxazolomycin A. Organic Letters. 14: 5460-3. PMID 23061613 DOI: 10.1021/Ol302541J |
0.605 |
|
| 2012 |
Donohoe TJ, Pilgrim BS, Jones GR, Bassuto JA. Synthesis of substituted isoquinolines utilizing palladium-catalyzed α-arylation of ketones. Proceedings of the National Academy of Sciences of the United States of America. 109: 11605-8. PMID 22753504 DOI: 10.1073/Pnas.1206532109 |
0.521 |
|
| 2012 |
Donohoe TJ, Bower JF, Chan LK. Olefin cross-metathesis for the synthesis of heteroaromatic compounds. Organic & Biomolecular Chemistry. 10: 1322-8. PMID 22215025 DOI: 10.1039/C2Ob06659A |
0.691 |
|
| 2012 |
Donohoe TJ, Kabeshov MA, Rathi AH, Smith IE. Direct preparation of thiazoles, imidazoles, imidazopyridines and thiazolidines from alkenes. Organic & Biomolecular Chemistry. 10: 1093-101. PMID 22159268 DOI: 10.1039/C1Ob06587D |
0.476 |
|
| 2012 |
Panchompoo J, Aldous L, Kabeshov M, Pilgrim BS, Donohoe TJ, Compton RG. A green approach to Fenton chemistry: Mono-hydroxylation of salicylic acid in aqueous medium by the electrogeneration of Fenton's reagent New Journal of Chemistry. 36: 1265-1272. DOI: 10.1039/C2Nj21007J |
0.324 |
|
| 2012 |
Donohoe TJ, Callens CKA, Lacy AR, Winter C. Tethered Aminohydroxylation Reaction and Its Application to Total Synthesis (Eur. J. Org. Chem. 4/2012) European Journal of Organic Chemistry. 2012: n/a-n/a. DOI: 10.1002/Ejoc.201290003 |
0.44 |
|
| 2012 |
Donohoe TJ, Callens CKA, Lacy AR, Winter C. Tethered aminohydroxylation reaction and its application to total synthesis European Journal of Organic Chemistry. 655-663. DOI: 10.1002/Ejoc.201101464 |
0.44 |
|
| 2011 |
Donohoe TJ, Jones CR, Barbosa LC. Total synthesis of (±)-streptonigrin: de novo construction of a pentasubstituted pyridine using ring-closing metathesis. Journal of the American Chemical Society. 133: 16418-21. PMID 21942896 DOI: 10.1021/Ja207835W |
0.644 |
|
| 2011 |
Donohoe TJ, Lacy AR, Rathi AH, Walter DS. The influence of exocyclic stereochemistry on the tethered aminohydroxylation reaction. Chemistry, An Asian Journal. 6: 3214-22. PMID 21919211 DOI: 10.1002/Asia.201100497 |
0.483 |
|
| 2011 |
Donohoe TJ, Bower JF, Baker DB, Basutto JA, Chan LK, Gallagher P. Synthesis of 2,4,6-trisubstituted pyridines via an olefin cross-metathesis/Heck-cyclisation-elimination sequence. Chemical Communications (Cambridge, England). 47: 10611-3. PMID 21870019 DOI: 10.1039/C1Cc14257G |
0.718 |
|
| 2011 |
Donohoe TJ, Winship PC, Tatton MR, Szeto P. A short and efficient synthesis of neodysiherbaine A by using catalytic oxidative cyclization. Angewandte Chemie (International Ed. in English). 50: 7604-6. PMID 21710669 DOI: 10.1002/Anie.201102525 |
0.416 |
|
| 2011 |
Donohoe TJ, Jahanshahi A, Tucker MJ, Bhatti FL, Roslan IA, Kabeshov M, Wrigley G. Exerting control over the acyloin reaction. Chemical Communications (Cambridge, England). 47: 5849-51. PMID 21503291 DOI: 10.1039/C1Cc11654A |
0.397 |
|
| 2011 |
Donohoe TJ, Connolly MJ, Rathi AH, Walton L. Intramolecular hydride addition to pyridinium salts: new routes to enantiopure dihydropyridones. Organic Letters. 13: 2074-7. PMID 21417360 DOI: 10.1021/Ol200478P |
0.485 |
|
| 2011 |
Donohoe TJ, Basutto JA, Bower JF, Rathi A. Heteroaromatic synthesis via olefin cross-metathesis: entry to polysubstituted pyridines. Organic Letters. 13: 1036-9. PMID 21268598 DOI: 10.1021/Ol103088R |
0.728 |
|
| 2011 |
Donohoe TJ, Callens CK, Flores A, Lacy AR, Rathi AH. Recent developments in methodology for the direct oxyamination of olefins. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 58-76. PMID 21207600 DOI: 10.1002/Chem.201002323 |
0.392 |
|
| 2011 |
Bataille CJ, Donohoe TJ. Osmium-free direct syn-dihydroxylation of alkenes. Chemical Society Reviews. 40: 114-28. PMID 21049111 DOI: 10.1039/B923880H |
0.367 |
|
| 2011 |
Donohoe TJ, Winship PCM, Tatton MR, Szeto P. Synthesis of (-)-Neodysiherbaine A Synfacts. 2011: 1048-1048. DOI: 10.1055/S-0030-1261142 |
0.459 |
|
| 2011 |
Meng Y, Aldous L, Pilgrim BS, Donohoe TJ, Compton RG. Palladium nanoparticle-modified carbon nanotubes for electrochemical hydrogenolysis in ionic liquids New Journal of Chemistry. 35: 1369-1375. DOI: 10.1039/C1Nj20070D |
0.344 |
|
| 2011 |
Terazzi E, Guénée L, Varin J, Bocquet B, Lemonnier J, Emery D, Mareda J, Piguet C, Barin G, Coskun A, Friedman DC, Olson MA, Colvin MT, Carmielli R, Dey SK, ... ... Donohoe TJ, et al. Cover Picture: Silver Baits for The “Miraculous Draught” of Amphiphilic Lanthanide Helicates / A Multistate Switchable [3]Rotacatenane / Heuristic Chemistry-Addition Reactions / Steric, Electronic, and Secondary Effects on the Coordination Chemistry of Io Chemistry - a European Journal. 17: 1-1. DOI: 10.1002/Chem.201090247 |
0.371 |
|
| 2011 |
Donohoe TJ, Bataille CJR, Innocenti P. Hydrogen-bonding-mediated directed osmium dihydroxylation Organic Reactions. 76: 1-48. DOI: 10.1002/0471264180.Or076.01 |
0.399 |
|
| 2010 |
Donohoe TJ, Bower JF, Basutto JA. Olefin cross-metathesis-based approaches to furans: procedures for the preparation of di- and trisubstituted variants. Nature Protocols. 5: 2005-10. PMID 21127493 DOI: 10.1038/Nprot.2010.147 |
0.708 |
|
| 2010 |
Donohoe TJ, Winship PC, Pilgrim BS, Walter DS, Callens CK. A novel oxidative cyclisation onto vinyl silanes. Chemical Communications (Cambridge, England). 46: 7310-2. PMID 20830333 DOI: 10.1039/C0Cc01342K |
0.411 |
|
| 2010 |
Donohoe TJ, Race NJ, Bower JF, Callens CK. Substituted pyrroles via olefin cross-metathesis. Organic Letters. 12: 4094-7. PMID 20712303 DOI: 10.1021/Ol101681R |
0.668 |
|
| 2010 |
Donohoe TJ, Bower JF. An expedient route to substituted furans via olefin cross-metathesis. Proceedings of the National Academy of Sciences of the United States of America. 107: 3373-6. PMID 20142508 DOI: 10.1073/Pnas.0913466107 |
0.716 |
|
| 2010 |
Donohoe TJ, Lindsay-Scott PJ, Parker JS, Callens CK. New modes for the osmium-catalyzed oxidative cyclization. Organic Letters. 12: 1060-3. PMID 20136133 DOI: 10.1021/Ol100046A |
0.444 |
|
| 2010 |
Donohoe TJ, Kabeshov MA, Rathi AH, Smith IED. Direct preparation of heteroaromatic compounds from alkenes Synlett. 2956-2958. DOI: 10.1055/S-0030-1259034 |
0.464 |
|
| 2010 |
Donohoe TJ, Lindsay-Scott PJ, Parker JS, Callens CKA. Synthesis of Pyrrolidines by Osmium-Catalyzed Oxidative Cyclization Synfacts. 2010: 683-683. DOI: 10.1055/S-0029-1219968 |
0.442 |
|
| 2010 |
Donohoe TJ, Brian PM, Hargaden GC, O'Riordan TJC. Synthesis of cylindricine C and a formal synthesis of cylindricine A Tetrahedron. 66: 6411-6420. DOI: 10.1016/J.Tet.2010.05.044 |
0.454 |
|
| 2010 |
MAGNUS P, BOOTH J, DIORAZIO L, DONOHOE T, LYNCH V, MAGNUS N, MENDOZA J, PYE P, TARRANT J. ChemInform Abstract: Taxane Diterpenes. Part 2. Synthesis of the 7-Deoxy ABC Taxane Skeleton, and Reactions of the A-Ring. Cheminform. 28: no-no. DOI: 10.1002/chin.199710156 |
0.429 |
|
| 2010 |
MAGNUS P, DIORAZIO L, DONOHOE T, GILES M, PYE P, TARRANT J, THOM S. ChemInform Abstract: New Strategy for the Synthesis of the Taxane Diterpenes: Formation of the Eight-Membered B-Ring of Taxol by Semi-Pinacol Rearrangement. Cheminform. 27: no-no. DOI: 10.1002/chin.199608206 |
0.341 |
|
| 2010 |
BAUTA W, BOOTH J, BOS ME, DELUCA M, DIORAZIO L, DONOHOE T, MAGNUS N, MAGNUS P, MENDOZA J, PYE P, TARRANT J, THOM S, UJJAINWALLA F. ChemInform Abstract: New Strategy for the Synthesis of the Taxane Diterpenes: Formation of the BC-Rings of Taxol via a (5 + 2) Pyrylium Ylide-Alkene Cyclization, Ring Expansion Strategy. Cheminform. 26: no-no. DOI: 10.1002/chin.199544208 |
0.368 |
|
| 2010 |
DAVIES SG, DONOHOE TJ. ChemInform Abstract: Arene Chromium Tricarbonyl Stabilized Benzylic Carbocations Cheminform. 25: no-no. DOI: 10.1002/chin.199407310 |
0.385 |
|
| 2009 |
Donohoe TJ, Winship PC, Walter DS. A Lewis acid promoted oxidative cyclization. The Journal of Organic Chemistry. 74: 6394-7. PMID 20560576 DOI: 10.1021/Jo901243Y |
0.37 |
|
| 2009 |
Demuner AJ, Valente VM, Barbosa LC, Rathi AH, Donohoe TJ, Thompson AL. Synthesis and phytotoxic activity of new pyridones derived from 4-hydroxy-6-methylpyridin-2(1H)-one. Molecules (Basel, Switzerland). 14: 4973-86. PMID 20032871 DOI: 10.3390/Molecules14124973 |
0.36 |
|
| 2009 |
Donohoe TJ, Connolly MJ, Walton L. Regioselective nucleophilic addition to pyridinium salts: a new route to substituted dihydropyridones. Organic Letters. 11: 5562-5. PMID 19891431 DOI: 10.1021/Ol902402V |
0.43 |
|
| 2009 |
Donohoe TJ, Harris RM, Williams O, Hargaden GC, Burrows J, Parker J. Concise syntheses of the natural products (+)-sylvaticin and (+)-cis-sylvaticin. Journal of the American Chemical Society. 131: 12854-61. PMID 19673528 DOI: 10.1021/Ja9049959 |
0.417 |
|
| 2009 |
Donohoe TJ, Flores A, Bataille CJ, Churruca F. Synthesis of (-)-hygromycin A: application of Mitsunobu glycosylation and tethered aminohydroxylation. Angewandte Chemie (International Ed. in English). 48: 6507-10. PMID 19650101 DOI: 10.1002/Anie.200902840 |
0.411 |
|
| 2009 |
Donohoe TJ, Wheelhouse KM, Lindsay-Scott PJ, Churchill GH, Connolly MJ, Butterworth S, Glossop PA. Osmium-mediated oxidative cyclizations: a study into the range of initiators that facilitate cyclization. Chemistry, An Asian Journal. 4: 1237-47. PMID 19579254 DOI: 10.1002/Asia.200900168 |
0.506 |
|
| 2009 |
Donohoe TJ, Fishlock LP, Basutto JA, Bower JF, Procopiou PA, Thompson AL. Synthesis of substituted pyridines and pyridazines via ring closing metathesis. Chemical Communications (Cambridge, England). 3008-10. PMID 19462069 DOI: 10.1039/B904363B |
0.721 |
|
| 2009 |
Donohoe TJ, Callens CK, Thompson AL. Tethered aminohydroxylation (TA) reaction of amides. Organic Letters. 11: 2305-7. PMID 19419162 DOI: 10.1021/Ol900631Y |
0.485 |
|
| 2009 |
Donohoe TJ, O'Riordan TJ, Rosa CP. Ruthenium-catalyzed isomerization of terminal olefins: applications to synthesis. Angewandte Chemie (International Ed. in English). 48: 1014-7. PMID 19130520 DOI: 10.1002/Anie.200804617 |
0.472 |
|
| 2009 |
Donohoe TJ, Lindsay-Scott PJ, Parker JS. Tandem catalysis in the polycyclisation of dienes to produce multi-substituted tetrahydrofurans Tetrahedron Letters. 50: 3523-3526. DOI: 10.1016/J.Tetlet.2009.03.027 |
0.422 |
|
| 2009 |
Donohoe TJ, Bower JF, Basutto JA, Fishlock LP, Procopiou PA, Callens CKA. Ring-closing metathesis for the synthesis of heteroaromatics: evaluating routes to pyridines and pyridazines Tetrahedron. 65: 8969-8980. DOI: 10.1016/J.Tet.2009.07.076 |
0.724 |
|
| 2009 |
Donohoe TJ, Kershaw NM, Baron R, Compton RG. The effect of ortho-substitution on the efficacy of biphenyls in mediating electron transfer from lithium Tetrahedron. 65: 5377-5384. DOI: 10.1016/J.Tet.2009.04.057 |
0.327 |
|
| 2009 |
Baron R, Kershaw NM, Donohoe TJ, Compton RG. Quantitative voltammetry of the reduction of methyl benzoate in thf reveals strong ion pairing of the radical anion with tetra-n-butyl cations Journal of Physical Organic Chemistry. 22: 247-253. DOI: 10.1002/Poc.1462 |
0.305 |
|
| 2009 |
Donohoe T, O'Riordan T, Rosa C. Ruthenium-katalysierte Isomerisierung von terminalen Olefinen: Anwendungen in der Synthese Angewandte Chemie. 121: 1032-1035. DOI: 10.1002/Ange.200804617 |
0.381 |
|
| 2008 |
Donohoe TJ, Cheeseman MD, O'Riordan TJ, Kershaw JA. Synthesis of (+)-DGDP and (-)-7-epialexine. Organic & Biomolecular Chemistry. 6: 3896-8. PMID 18931792 DOI: 10.1039/B815332A |
0.483 |
|
| 2008 |
Rees NV, Baron R, Kershaw NM, Donohoe TJ, Compton RG. Alkali metal reductions of organic molecules: why mediated electron transfer from lithium is faster than direct reduction. Journal of the American Chemical Society. 130: 12256-7. PMID 18714997 DOI: 10.1021/Ja805086W |
0.339 |
|
| 2008 |
Donohoe TJ, Ironmonger A, Kershaw NM. Synthesis of (-)-(Z)-deoxypukalide. Angewandte Chemie (International Ed. in English). 47: 7314-6. PMID 18688890 DOI: 10.1002/Anie.200802703 |
0.424 |
|
| 2008 |
Donohoe TJ, Thomas RE, Cheeseman MD, Rigby CL, Bhalay G, Linney ID. Flexible strategy for the synthesis of pyrrolizidine alkaloids. Organic Letters. 10: 3615-8. PMID 18636741 DOI: 10.1021/Ol801415D |
0.479 |
|
| 2008 |
Donohoe TJ, Fishlock LP, Procopiou PA. Ring-closing metathesis: novel routes to aromatic heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 5716-26. PMID 18381742 DOI: 10.1002/Chem.200800130 |
0.448 |
|
| 2008 |
Donohoe TJ, Wheelhouse KM, Lindsay-Scott PJ, Glossop PA, Nash IA, Parker JS. Pyridine-N-oxide as a mild reoxidant which transforms osmium-catalyzed oxidative cyclization. Angewandte Chemie (International Ed. in English). 47: 2872-5. PMID 18324650 DOI: 10.1002/Anie.200705425 |
0.306 |
|
| 2008 |
Donohoe TJ, Fishlock LP, Procopiou PA. A metathesis-based approach to the synthesis of 2-pyridones and pyridines. Organic Letters. 10: 285-8. PMID 18154343 DOI: 10.1021/Ol702684D |
0.506 |
|
| 2008 |
Donohoe TJ, Fishlock LP, Procopiou PA. Ring-closing metathesis as a key step in the synthesis of 2-pyridones and pyridine triflates Synthesis. 2665-2667. DOI: 10.1055/S-2008-1067180 |
0.468 |
|
| 2008 |
Donohoe TJ, Fishlock LP, Procopiou PA. Construction of 2-Pyridones and Pyridines via Ring-Closing Metathesis Synfacts. 2008: 345-345. DOI: 10.1055/S-2008-1042859 |
0.382 |
|
| 2008 |
Donohoe TJ, Kershaw NM, Orr AJ, Wheelhouse KMP, Fishlock L, Lacy AR, Bingham M, Procopiou PA. Flexible metathesis-based approaches to highly functionalised furans and pyrroles Tetrahedron. 64: 809-820. DOI: 10.1016/J.Tet.2007.09.087 |
0.454 |
|
| 2008 |
Donohoe TJ, Ironmonger A, Kershaw NM. ChemInform Abstract: Synthesis of (-)-(Z)-Deoxypukalide. Cheminform. 39. DOI: 10.1002/chin.200851180 |
0.331 |
|
| 2007 |
Donohoe TJ, Rosa CP. A concise and efficient synthesis of (-)-allosamizoline. Organic Letters. 9: 5509-11. PMID 18004864 DOI: 10.1021/ol702449m |
0.474 |
|
| 2007 |
Donohoe TJ, Thomas RE. The partial reduction of electron-deficient pyrroles: procedures describing both Birch (Li/NH3) and ammonia-free (Li/DBB) conditions. Nature Protocols. 2: 1888-95. PMID 17703200 DOI: 10.1038/Nprot.2007.245 |
0.445 |
|
| 2007 |
Donohoe TJ, Thomas RE. Partial reduction of pyrroles: application to natural product synthesis. Chemical Record (New York, N.Y.). 7: 180-90. PMID 17549705 DOI: 10.1002/Tcr.20115 |
0.509 |
|
| 2007 |
Donohoe TJ, Bataille CJ, Gattrell W, Kloesges J, Rossignol E. Tethered aminohydroxylation: dramatic improvements to the process. Organic Letters. 9: 1725-8. PMID 17388605 DOI: 10.1021/Ol070430V |
0.43 |
|
| 2007 |
Donohoe TJ, Fishlock LP, Lacy AR, Procopiou PA. A metathesis-based approach to the synthesis of furans. Organic Letters. 9: 953-6. PMID 17316009 DOI: 10.1021/Ol062933R |
0.535 |
|
| 2007 |
Donohoe TJ, Chiu JY, Thomas RE. Synthesis of the pyrrolidinone core of KSM-2690 B. Organic Letters. 9: 421-4. PMID 17249777 DOI: 10.1021/Ol062705X |
0.464 |
|
| 2007 |
Paddon CA, Bhatti FL, Donohoe TJ, Compton RG. Electrosynthetic reduction of 1-iodoadamantane forming 1,1'-biadamantane and adamantane in aprotic solvents: insonation switches the mechanism from dimerisation to exclusive monomer formation. Ultrasonics Sonochemistry. 14: 502-8. PMID 17224295 DOI: 10.1016/J.Ultsonch.2006.11.007 |
0.366 |
|
| 2007 |
Donohoe T, Churchill G, Wheelhouse K, Glossop P. Catalytic Oxidative Cyclizations Mediated by Osmium Synfacts. 2007: 0279-0279. DOI: 10.1055/S-2007-968249 |
0.321 |
|
| 2007 |
Donohoe TJ, Thomas RE. Formation of N -Boc pyrrole 2,5-methyl diester, a key intermediate in the Donohoe synthesis of 1-epiaustraline and hyacinthacine A 1 . Nature Protocols. DOI: 10.1038/Nprot.2007.232 |
0.397 |
|
| 2007 |
Donohoe TJ, Thomas RE. Formation of N -Boc pyrrole 2-ethyl ester, a key intermediate in the Donohoe synthesis of omuralide. Nature Protocols. DOI: 10.1038/Nprot.2007.231 |
0.44 |
|
| 2007 |
Wood NCL, Paddon CA, Bhatti FL, Donohoe TJ, Compton RG. Mediated electron transfer from lithium investigated voltammetrically in tetrahydrofuran: Why are some mediators more effective reducing reagents than others? Journal of Physical Organic Chemistry. 20: 732-742. DOI: 10.1002/Poc.1232 |
0.39 |
|
| 2007 |
Burasov AV, Paddon CA, Bhatti EL, Donohoe TJ, Compton RG. Cryoelectrochemical reduction of a phenyl sulfide in tetrahydrofuran: Mediated reduction gives different products compared to direct reduction Journal of Physical Organic Chemistry. 20: 144-150. DOI: 10.1002/Poc.1138 |
0.357 |
|
| 2006 |
Donohoe TJ, Churchill GH, Wheelhouse KM, Glossop PA. Stereoselective synthesis of pyrrolidines: catalytic oxidative cyclizations mediated by osmium. Angewandte Chemie (International Ed. in English). 45: 8025-8. PMID 17083141 DOI: 10.1002/Anie.200603240 |
0.445 |
|
| 2006 |
Donohoe TJ, Harris RM, Burrows J, Parker J. Total synthesis of (+)-cis-sylvaticin: double oxidative cyclization reactions catalyzed by osmium. Journal of the American Chemical Society. 128: 13704-5. PMID 17044695 DOI: 10.1021/Ja0660148 |
0.436 |
|
| 2006 |
Paddon CA, Bhatti FL, Donohoe TJ, Compton RG. Cryovoltammetrically probing functional group reductive cleavage: alkyl-sulfur versus aryl-sulfur bond cleavage in an alkyl naphthyl thioether under single electron-transfer is temperature switchable. Chemical Communications (Cambridge, England). 3402-4. PMID 16896475 DOI: 10.1039/B606638K |
0.379 |
|
| 2006 |
Donohoe TJ, Rigby CL, Thomas RE, Nieuwenhuys WF, Bhatti FL, Cowley AR, Bhalay G, Linney ID. An enzymatic approach to the desymmetrization of disubstituted pyrrolines. The Journal of Organic Chemistry. 71: 6298-301. PMID 16872226 DOI: 10.1021/Jo060926A |
0.45 |
|
| 2006 |
Donohoe TJ, Harris RM, Butterworth S, Burrows JN, Cowley A, Parker JS. New osmium-based reagent for the dihydroxylation of alkenes. The Journal of Organic Chemistry. 71: 4481-9. PMID 16749777 DOI: 10.1021/Jo060301C |
0.359 |
|
| 2006 |
Donohoe TJ, Orr AJ, Bingham M. Ring-closing metathesis as a basis for the construction of aromatic compounds. Angewandte Chemie (International Ed. in English). 45: 2664-70. PMID 16548035 DOI: 10.1002/Anie.200503512 |
0.457 |
|
| 2006 |
Donohoe TJ, Johnson DJ, Mace LH, Thomas RE, Chiu JY, Rodrigues JS, Compton RG, Banks CE, Tomcik P, Bamford MJ, Ichihara O. The ammonia-free partial reduction of substituted pyridinium salts. Organic & Biomolecular Chemistry. 4: 1071-84. PMID 16525551 DOI: 10.1039/B517462G |
0.498 |
|
| 2006 |
Donohoe TJ, Chughtai MJ, Klauber DJ, Griffin D, Campbell AD. N-sulfonyloxy carbamates as reoxidants for the tethered aminohydroxylation reaction. Journal of the American Chemical Society. 128: 2514-5. PMID 16492017 DOI: 10.1021/Ja057389G |
0.437 |
|
| 2006 |
Donohoe TJ, Sintim HO, Sisangia L, Ace KW, Guyo PM, Cowley A, Harling JD. Synthesis of clastro-Lactacystin β-Lactone Synfacts. 2006: 99-99. DOI: 10.1055/S-2005-921775 |
0.32 |
|
| 2006 |
Donohoe TJ, Bataille CJR, Churchill GH. Highlights of natural product synthesis Annual Reports On the Progress of Chemistry - Section B. 102: 98-122. DOI: 10.1039/B515095G |
0.362 |
|
| 2006 |
Fietkau N, Paddon CA, Bhatti FL, Donohoe TJ, Compton RG. Cryo-electrochemistry in tetrahydrofuran: The regioselective electrochemical reduction of a phenyl sulfone: Fast-scan cyclic voltammetry investigations Journal of Electroanalytical Chemistry. 593: 131-141. DOI: 10.1016/J.Jelechem.2006.03.004 |
0.308 |
|
| 2006 |
Paddon CA, Bhatti FL, Donohoe TJ, Compton RG. Cryo-electrochemistry in tetrahydrofuran: The electrochemical reduction of a phenyl thioether: [(3-{[trans-4-(Methoxymethoxy)cyclohexyl]oxy}propyl)thio]benzene Journal of Electroanalytical Chemistry. 589: 187-194. DOI: 10.1016/J.Jelechem.2006.02.010 |
0.404 |
|
| 2005 |
Donohoe TJ, Sintim HO, Hollinshead J. A noncarbohydrate based approach to polyhydroxylated pyrrolidizines: total syntheses of the natural products hyacinthacine A1 and 1-epiaustraline. The Journal of Organic Chemistry. 70: 7297-304. PMID 16122251 DOI: 10.1021/Jo050977S |
0.686 |
|
| 2005 |
Donohoe TJ, Butterworth S. Oxidative cyclization of diols derived from 1,5-dienes: formation of enantiopure cis-tetrahydrofurans by using catalytic osmium tetroxide; formal synthesis of (+)-cis-solamin. Angewandte Chemie (International Ed. in English). 44: 4766-8. PMID 15988770 DOI: 10.1002/Anie.200500513 |
0.375 |
|
| 2005 |
Donohoe TJ, Sintim HO, Sisangia L, Ace KW, Guyo PM, Cowley A, Harling JD. Utility of the ammonia-free Birch reduction of electron-deficient pyrroles: total synthesis of the 20s proteasome inhibitor, clasto-lactacystin beta-lactone. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 4227-38. PMID 15864801 DOI: 10.1002/Chem.200401119 |
0.7 |
|
| 2005 |
Donohoe TJ, Johnson PD, Pye RJ, Keenan M. Concise and enantioselective synthesis of the aminocyclitol core of hygromycin A. Organic Letters. 7: 1275-7. PMID 15787485 DOI: 10.1021/Ol0473750 |
0.493 |
|
| 2005 |
Donohoe TJ, Johnson DJ, Mace LH, Bamford MJ, Ichihara O. Partial reduction of pyridinium salts as a versatile route to dihydropyridones. Organic Letters. 7: 435-7. PMID 15673258 DOI: 10.1021/Ol0476624 |
0.505 |
|
| 2005 |
Banks CE, Evans RG, Rodrigues J, Turner PG, Donohoe TJ, Compton RG. Cryoelectrochemistry: Electrochemical reduction of 2(RS)-methyl 1-(tert-butoxycarbonyl)-2-iodomethyl-2,5-dihydropyrrole-2-carboxylate Tetrahedron. 61: 2365-2372. DOI: 10.1016/J.Tet.2005.01.022 |
0.449 |
|
| 2005 |
Donohoe TJ, Orr AJ, Gosby K, Bingham M. A metathesis approach to aromatic heterocycles European Journal of Organic Chemistry. 1969-1971. DOI: 10.1002/Ejoc.200500113 |
0.51 |
|
| 2005 |
Donohoe TJ, Butterworth S. Oxidative Cyclization of Diols Derived from 1,5-Dienes: Formation of Enantiopure cis-Tetrahydrofurans by Using Catalytic Osmium Tetroxide — Formal Synthesis of (+)-(IX). Cheminform. 36. DOI: 10.1002/chin.200547104 |
0.325 |
|
| 2004 |
Donohoe TJ, Freestone GC, Headley CE, Rigby CL, Cousins RP, Bhalay G. Enantioselective partial reduction of 2,5-disubstituted pyrroles via a chiral protonation approach. Organic Letters. 6: 3055-8. PMID 15330586 DOI: 10.1021/Ol049014Q |
0.44 |
|
| 2004 |
Donohoe TJ, Johnson PD, Pye RJ, Keenan M. Efficient acyclic stereocontrol using the tethered aminohydroxylation reaction. Organic Letters. 6: 2583-5. PMID 15255696 DOI: 10.1021/Ol049136I |
0.452 |
|
| 2004 |
Turner PG, Donohoe TJ, Cousins RP. Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: radical ring-expansion to substituted tetrahydropyridines. Chemical Communications (Cambridge, England). 1422-3. PMID 15179495 DOI: 10.1039/B404002C |
0.388 |
|
| 2004 |
Donohoe TJ, Sintim HO. A concise total synthesis of (+/-)-1-epiaustraline. Organic Letters. 6: 2003-6. PMID 15176804 DOI: 10.1021/Ol049397S |
0.657 |
|
| 2004 |
Donohoe TJ, Sintim HO, Sisangia L, Harling JD. An efficient synthesis of lactacystin beta-lactone. Angewandte Chemie (International Ed. in English). 43: 2293-6. PMID 15108149 DOI: 10.1002/Anie.200453843 |
0.572 |
|
| 2004 |
Carbery DR, Donohoe TJ. Enantiopure oxazolidinones as chiral acids in the asymmetric protonation of N-Boc pyrrole derived enolates. Chemical Communications (Cambridge, England). 722-3. PMID 15010799 DOI: 10.1039/B316719D |
0.383 |
|
| 2004 |
Donohoe TJ, Fisher JW, Edwards PJ. Synthesis of (+/-)-secosyrin 1 and a formal synthesis of (-)-secosyrin 1. Organic Letters. 6: 465-7. PMID 14961599 DOI: 10.1021/Ol0362313 |
0.558 |
|
| 2004 |
Donohoe TJ, Johnson DJ, Compton RG, Wadhawan JD. Low temperature electrochemistry as a mechanistic probe for the partial reduction of heterocycles Tetrahedron. 60: 5945-5952. DOI: 10.1016/J.Tet.2004.05.027 |
0.3 |
|
| 2004 |
Donohoe TJ, Sintim HO, Sisangia L, Harling JD. An Efficient Synthesis of Lactacystinβ-Lactone Angewandte Chemie. 116: 2343-2346. DOI: 10.1002/Ange.200453843 |
0.639 |
|
| 2003 |
Donohoe TJ, Logan JG, Laffan DD. Trichloro-oxazolines as activated donors for aminosugar coupling. Organic Letters. 5: 4995-8. PMID 14682748 DOI: 10.1021/Ol0359620 |
0.391 |
|
| 2003 |
Donohoe TJ, House D, Ace KW. Scope of the reductive aldol reaction: application to aromatic carbocycles and heterocycles. Organic & Biomolecular Chemistry. 1: 3749-57. PMID 14649906 DOI: 10.1039/B306937K |
0.464 |
|
| 2003 |
Donohoe TJ, Mitchell L, Waring MJ, Helliwell M, Bell A, Newcombe NJ. Scope of the directed dihydroxylation: application to cyclic homoallylic alcohols and trihaloacetamides. Organic & Biomolecular Chemistry. 1: 2173-86. PMID 12945911 DOI: 10.1039/B303081D |
0.681 |
|
| 2003 |
Donohoe TJ, Johnson PD, Pye RJ. The tethered aminohydroxylation (TA) reaction. Organic & Biomolecular Chemistry. 1: 2025-8. PMID 12945888 DOI: 10.1039/B305189G |
0.393 |
|
| 2003 |
Donohoe TJ, Headley CE, Cousins RP, Cowley A. Flexibility in the partial reduction of 2,5-disubstituted pyrroles: application to the synthesis of DMDP. Organic Letters. 5: 999-1002. PMID 12659558 DOI: 10.1021/Ol027504H |
0.495 |
|
| 2003 |
Donohoe TJ, Butterworth S. A general oxidative cyclization of 1,5-dienes using catalytic osmium tetroxide. Angewandte Chemie (International Ed. in English). 42: 948-51. PMID 12596187 DOI: 10.1002/Anie.200390253 |
0.337 |
|
| 2003 |
Donohoe TJ, House D. Diastereoselective reductive aldol reactions of Boc-protected electron deficient pyrroles Tetrahedron Letters. 44: 1095-1098. DOI: 10.1016/S0040-4039(02)02672-2 |
0.464 |
|
| 2002 |
Donohoe TJ, Blades K, Moore PR, Waring MJ, Winter JJ, Helliwell M, Newcombe NJ, Stemp G. Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA. The Journal of Organic Chemistry. 67: 7946-56. PMID 12423122 DOI: 10.1021/Jo026161Y |
0.673 |
|
| 2002 |
Donohoe TJ, Johnson PD, Cowley A, Keenan M. The tethered aminohydroxylation (TA) of cyclic allylic carbamates. Journal of the American Chemical Society. 124: 12934-5. PMID 12405805 DOI: 10.1021/Ja0276117 |
0.441 |
|
| 2002 |
Donohoe TJ, Raoof A, Freestone GC, Linney ID, Cowley A, Helliwell M. Synthesis of enantiopure dihydropyranones: aldol-based ring expansion of dihydrofurans. Organic Letters. 4: 3059-62. PMID 12201716 DOI: 10.1021/Ol0263595 |
0.52 |
|
| 2002 |
Donohoe TJ, House D. Ammonia free partial reduction of aromatic compounds using lithium di-tert-butylbiphenyl (LiDBB). The Journal of Organic Chemistry. 67: 5015-8. PMID 12098328 DOI: 10.1021/Jo0257593 |
0.385 |
|
| 2002 |
Donohoe TJ. Development of the directed dihydroxylation reaction Synlett. 1223-1232. DOI: 10.1055/S-2002-32947 |
0.484 |
|
| 2002 |
Donohoe TJ, Mace L, Helliwell M, Ichihara O. Transformations of 3,4-disubstituted pyridines under dissolving metal conditions - Partial reduction followed by radical cyclisation Synlett. 331-333. DOI: 10.1055/S-2002-19757 |
0.465 |
|
| 2002 |
Donohoe TJ, Calabrese AA, Guillermin JB, Frampton CS, Walter D. Partial reduction of 3-heteroatom substituted 2-furoic acids: The role of an ortho group in viability and stereoselectivity Journal of the Chemical Society. Perkin Transactions 1. 1748-1756. DOI: 10.1039/B203437A |
0.494 |
|
| 2002 |
Donohoe TJ, Guillermin JB, Walter DS. Preparation of (+)-nemorensic acid and approaches to nemorensine using the partial reduction of electron deficient furans Journal of the Chemical Society. Perkin Transactions 1. 1369-1375. DOI: 10.1039/B202514K |
0.491 |
|
| 2001 |
Donohoe TJ, Johnson PD, Helliwell M, Keenan M. The regioselective aminohydroxylation of allylic carbamates. Chemical Communications (Cambridge, England). 2078-9. PMID 12240171 DOI: 10.1039/B107253F |
0.389 |
|
| 2001 |
Donohoe TJ, Raoof A, Linney ID, Helliwell M. Partial reduction of annulated heterocycles as a general route to medium rings containing oxygen and nitrogen. Organic Letters. 3: 861-4. PMID 11263901 DOI: 10.1021/Ol007035O |
0.52 |
|
| 2001 |
Donohoe TJ, McRiner AJ, Helliwell M, Sheldrakeb P. Use of dissolving metals in the partial reduction of pyridines: Formation of 2-alkyl-1,2-dihydropyridines Journal of the Chemical Society. Perkin Transactions 1. 1435-1445. DOI: 10.1039/B101662H |
0.406 |
|
| 2001 |
Donohoe TJ, Mitchell L, Waring MJ, Helliwell M, Bell A, Newcombe NJ. Homoallylic alcohols and trichloroacetamides as hydrogen bond donors for directed dihydroxylation Tetrahedron Letters. 42: 8951-8954. DOI: 10.1016/S0040-4039(01)01999-2 |
0.678 |
|
| 2001 |
Donohoe TJ, Guillermin JB, Calabrese AA, Walter DS. Silyl substituted furans in the stereoselective Birch reduction Tetrahedron Letters. 42: 5841-5844. DOI: 10.1016/S0040-4039(01)01151-0 |
0.492 |
|
| 2001 |
Donohoe TJ, Winter JJG, Helliwell M, Stemp G. Hydrogen bonding control in the oxidative cyclisation of 1,5-dienes Tetrahedron Letters. 42: 971-974. DOI: 10.1016/S0040-4039(00)02225-5 |
0.523 |
|
| 2000 |
Donohoe TJ, McRiner AJ, Sheldrake P. Partial reduction of electron-deficient pyridines Organic Letters. 2: 3861-3. PMID 11101438 DOI: 10.1021/Ol0065930 |
0.441 |
|
| 2000 |
Donohoe TJ, Waring MJ, Newcombe NJ. Enhanced stereoselectivity in the catalytic dihydroxylation of acyclic allylic alcohols Synlett. 149-151. DOI: 10.1055/S-2000-6457 |
0.655 |
|
| 2000 |
Donohoe TJ, Calabrese AA, Stevenson CA, Ladduwahetty T. Stereoselective reduction of chiral 2-furoic acid derivatives using group I metals in ammonia Journal of the Chemical Society, Perkin Transactions 1. 3724-3731. DOI: 10.1039/B006390H |
0.412 |
|
| 2000 |
Donohoe TJ, Guillermin JB, Frampton C, Walter DS. The synthesis of (+)-nemorensic acid Chemical Communications. 465-466. DOI: 10.1039/B000565G |
0.414 |
|
| 2000 |
Donohoe TJ, Harji RR, Cousins RPC. The partial reduction of heterocycles: An alternative to the birch reduction Tetrahedron Letters. 41: 1331-1334. DOI: 10.1016/S0040-4039(99)02315-1 |
0.478 |
|
| 2000 |
Donohoe TJ, Harji RR, Cousins RPC. Stereoselective reductive alkylation of 2,5-disubstituted pyrroles: A role for naphthalene in the partial reduction of heterocycles Tetrahedron Letters. 41: 1327-1330. DOI: 10.1016/S0040-4039(99)02314-X |
0.466 |
|
| 2000 |
Donohoe TJ, Ace KW, Guyo PM, Helliwell M, McKenna J. Reductive aldol reactions on aromatic heterocycles Tetrahedron Letters. 41: 989-993. DOI: 10.1016/S0040-4039(99)02224-8 |
0.464 |
|
| 2000 |
Blades K, Donohoe TJ, Winter JJG, Stemp G. A syn selective dihydroxylation of cyclic allylic trichloroacetamides using catalytic osmium tetroxide Tetrahedron Letters. 41: 4701-4704. DOI: 10.1016/S0040-4039(00)00714-0 |
0.37 |
|
| 2000 |
Donohoe TJ, Guyo PM, Raoof A. ChemInform Abstract: Birch Reduction of Aromatic Heterocycles Cheminform. 31: no-no. DOI: 10.1002/chin.200050283 |
0.314 |
|
| 1999 |
Donohoe TJ, Blades K, Helliwell M, Moore PR, Winter JJ, Stemp G. Directed Dihydroxylation of Allylic Trichloroacetamides. The Journal of Organic Chemistry. 64: 2980-2981. PMID 11674383 DOI: 10.1021/Jo982468E |
0.383 |
|
| 1999 |
Donohoe TJ, Blades K, Helliwell M. Synthesis of amino-sugars using the directed dihydroxylation reaction Chemical Communications. 1733-1734. DOI: 10.1039/A904991F |
0.465 |
|
| 1999 |
Donohoe TJ, Harji RR, Cousins RPC. Stereoselectivity in the double reductive alkylation of pyrroles: Synthesis of cis-3,4-disubstituted pyrrolidines Chemical Communications. 141-142. DOI: 10.1039/A809193E |
0.48 |
|
| 1999 |
Donohoe TJ, Stevenson CA, Helliwell M, Irshad R, Ladduwahetty T. The synthesis of (-)-cis- and (-)-trans-crobarbatic acid Tetrahedron Asymmetry. 10: 1315-1322. DOI: 10.1016/S0957-4166(99)00097-X |
0.443 |
|
| 1999 |
Donohoe TJ, Newcombe NJ, Waring MJ. syn Stereocontrol in the directed dihydroxylation of acyclic allylic alcohols Tetrahedron Letters. 40: 6881-6885. DOI: 10.1016/S0040-4039(99)01371-4 |
0.687 |
|
| 1999 |
Donohoe TJ, Guyo PM, Helliwell M. The stereoselective Birch reduction of pyrroles Tetrahedron Letters. 40: 435-438. DOI: 10.1016/S0040-4039(98)02395-8 |
0.44 |
|
| 1998 |
Donohoe TJ, Guyo PM, Beddoes RL, Helliwell M. Reduction of electron-deficient pyrroles using group I and II metals in ammonia Journal of the Chemical Society - Perkin Transactions 1. 667-676. DOI: 10.1039/A707661D |
0.447 |
|
| 1998 |
Donohoe TJ, Harji RR, Moore PR, Waring MJ. Applications of stoichiometric organotransition metal complexes in organic synthesis Journal of the Chemical Society - Perkin Transactions 1. 819-834. DOI: 10.1039/A706382B |
0.626 |
|
| 1998 |
Donohoe TJ, Blades K, Helliwell M, Waring MJ, Newcombe NJ. The synthesis of (+)-pericosine B Tetrahedron Letters. 39: 8755-8758. DOI: 10.1016/S0040-4039(98)01989-3 |
0.709 |
|
| 1998 |
Donohoe TJ, Guyo PM, Harji RR, Helliwell M, Cousins RPC. The Birch reduction of 3-substituted pyrroles Tetrahedron Letters. 39: 3075-3078. DOI: 10.1016/S0040-4039(98)00362-1 |
0.494 |
|
| 1998 |
Donohoe TJ, Helliwell M, Stevenson CA, Ladduwahetty T. Stereoselectivity in the Birch reduction of 2-furoic acid derivatives Tetrahedron Letters. 39: 3071-3074. DOI: 10.1016/S0040-4039(98)00361-X |
0.384 |
|
| 1997 |
Donohoe TJ, Moore PR, Beddoes RL. Studies on the role of conformation and of hydrogen-bonding on the dihydroxylation of cyclic allylic alcohols: Application to the synthesis of conduritol D Journal of the Chemical Society - Perkin Transactions 1. 43-51. DOI: 10.1039/A604052G |
0.428 |
|
| 1997 |
Donohoe TJ, Moore PR, Waring MJ, Newcombe NJ. The directed dihydroxylation of allylic alcohols Tetrahedron Letters. 38: 5027-5030. DOI: 10.1016/S0040-4039(97)01061-7 |
0.673 |
|
| 1996 |
Donohoe TJ, Garg R, Stevenson CA. Prospects for stereocontrol in the reduction of aromatic compounds Tetrahedron Asymmetry. 7: 317-344. DOI: 10.1016/0957-4166(96)00001-8 |
0.304 |
|
| 1996 |
Donohoe TJ, Garg R, Moore PR. On the dihydroxylation of cyclic allylic alcohols Tetrahedron Letters. 37: 3407-3410. DOI: 10.1016/0040-4039(96)00558-8 |
0.421 |
|
| 1996 |
Bauta WE, Booth J, Bos ME, DeLuca M, Diorazio L, Donohoe TJ, Frost C, Magnus N, Magnus P, Mendoza J, Pye P, Tarrant JG, Thom S, Ujjainwalla F. Taxane diterpenes 1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors Tetrahedron. 52: 14081-14102. DOI: 10.1016/0040-4020(96)00867-8 |
0.706 |
|
| 1996 |
Magnus P, Booth J, Diorazio L, Donohoe T, Lynch V, Magnus N, Mendoza J, Pye P, Tarrant J. Taxane diterpenes 2: Synthesis of the 7-deoxy ABC taxane skeleton, and reactions of the A-ring Tetrahedron. 52: 14103-14146. DOI: 10.1016/0040-4020(96)00866-6 |
0.738 |
|
| 1996 |
Magnus P, Diorazio L, Donohoe TJ, Giles M, Pye P, Tarrant J, Thom S. Taxane diterpenes 3: Formation of the eight-membered B-ring by semi-pinacol rearrangement Tetrahedron. 52: 14147-14176. DOI: 10.1016/0040-4020(96)00865-4 |
0.697 |
|
| 1995 |
Magnus P, Diorazio L, Donohoe T, Giles M, Pye P, Tarrant J, Thom S. New strategy for the synthesis of the taxane diterpenes: formation of the eight-membered B-ring of taxol by semi-pinacol rearrangement Journal of the Chemical Society, Chemical Communications. 1935-1936. DOI: 10.1039/C39950001935 |
0.7 |
|
| 1995 |
Bauta W, Booth J, Bos ME, DeLuca M, Diorazio L, Donohoe T, Magnus N, Magnus P, Mendoza J, Pye P, Tarrant J, Thom S, Ujjainwalla F. New strategy for the synthesis of the taxane diterpenes: Formation of the BC-rings of taxol via a [5+2]-pyrylium ylide-alkene cyclization, ring expansion strategy Tetrahedron Letters. 36: 5327-5330. DOI: 10.1016/0040-4039(95)01083-T |
0.721 |
|
| 1993 |
Davies SG, Donohoe TJ. Arene Chromium Tricarbonyl Stabilised Benzylic Carbocations Synlett. 1993: 323-332. DOI: 10.1055/S-1993-22443 |
0.556 |
|
| 1992 |
Davies SG, Donohoe TJ, Williams JMJ. Stereoselective manipulation of acetals derived from o-substituted benzaldehyde chromium tricarbonyl complexes Pure and Applied Chemistry. 64: 379-386. DOI: 10.1351/Pac199264030379 |
0.587 |
|
| 1991 |
Davies SG, Donohoe TJ, Lister MA. Asymmetric synthesis of 2-aryl-tetrahydropyrans via arene chromium tricarbonyl methodology 2: 2-Aryl-3-ethyl-4-chloro-tetrahydropyrans Tetrahedron: Asymmetry. 2: 1089-1092. DOI: 10.1016/S0957-4166(00)82003-0 |
0.468 |
|
| 1991 |
Davies SG, Donohoe TJ, Lister MA. Asymmetric synthesis of 2-aryl-tetrahydropyrans via arene chromium tricarbonyl methodology 1: cis-2-Aryl-4-chloro-tetrahydropyrans Tetrahedron: Asymmetry. 2: 1085-1088. DOI: 10.1016/S0957-4166(00)82002-9 |
0.334 |
|
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