Year |
Citation |
Score |
2024 |
Zhang Y, Zhang JJ, Lou L, Lin R, Cramer N, Wang SG, Chen Z. Recent advances in Rh(I)-catalyzed enantioselective C-H functionalization. Chemical Society Reviews. PMID 38411467 DOI: 10.1039/d3cs00762f |
0.388 |
|
2024 |
Zhang G, Wodrich MD, Cramer N. Catalytic enantioselective reductive Eschenmoser-Claisen rearrangements. Science (New York, N.Y.). 383: 395-401. PMID 38271525 DOI: 10.1126/science.adl3369 |
0.37 |
|
2023 |
Cao YX, Wodrich MD, Cramer N. Nickel-catalyzed direct stereoselective α-allylation of ketones with non-conjugated dienes. Nature Communications. 14: 7640. PMID 37993440 DOI: 10.1038/s41467-023-43197-z |
0.393 |
|
2023 |
Zhang G, Cramer N. Reductive Asymmetric Aza-Mislow-Evans Rearrangement by 1,3,2-Diazaphospholene Catalysis. Angewandte Chemie (International Ed. in English). e202301076. PMID 36820495 DOI: 10.1002/anie.202301076 |
0.758 |
|
2022 |
Tan JF, Bormann CT, Severin K, Cramer N. Chemo- and regio-divergent access to fluorinated 1-alkyl and 1-acyl triazenes from alkynyl triazenes. Chemical Science. 13: 3409-3415. PMID 35432853 DOI: 10.1039/d2sc00294a |
0.361 |
|
2022 |
Klett J, Woźniak Ł, Cramer N. 1,3,2-Diazaphospholene-Catalyzed Reductive Cyclizations of Organohalides. Angewandte Chemie (International Ed. in English). e202202306. PMID 35419901 DOI: 10.1002/anie.202202306 |
0.329 |
|
2021 |
Mas-Roselló J, Cramer N. Catalytic Reduction of Oximes to Hydroxylamines: Current Methods, Challenges and Opportunities. Chemistry (Weinheim An Der Bergstrasse, Germany). e202103683. PMID 34817089 DOI: 10.1002/chem.202103683 |
0.335 |
|
2021 |
Braconi E, Cramer N. Crossed Regio- and Enantioselective Iron-Catalyzed [4+2]-Cycloadditions of Unactivated Dienes. Angewandte Chemie (International Ed. in English). PMID 34708502 DOI: 10.1002/anie.202112148 |
0.306 |
|
2021 |
Tan JF, Bormann CT, Severin K, Cramer N. Alkynyl triazenes enable divergent syntheses of 2-pyrones. Chemical Science. 12: 9140-9145. PMID 34276943 DOI: 10.1039/d1sc02583j |
0.327 |
|
2021 |
Woźniak Ł, Cramer N. Atropo-Enantioselective Oxidation-Enabled Iridium(III)-Catalyzed C-H Arylations with Aryl Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 34153163 DOI: 10.1002/anie.202106403 |
0.442 |
|
2021 |
Cramer N, Mas-Roselló J, Cope CJ, Tan E, Pinson B, Robinson A, Smejkal T. Iridium-Catalyzed Acid-Assisted Hydrogenation of Oximes to Hydroxylamines. Angewandte Chemie (International Ed. in English). PMID 33886142 DOI: 10.1002/anie.202103806 |
0.304 |
|
2020 |
Braconi E, Götzinger AC, Cramer N. Enantioselective Iron-Catalyzed Cross-[4+4]-Cycloaddition of 1,3-Dienes Provides Chiral Cyclooctadienes. Journal of the American Chemical Society. PMID 33175501 DOI: 10.1021/jacs.0c09486 |
0.371 |
|
2020 |
Cramer N, Ozols K, Onodera S, Woźniak Ł. Cobalt(III)-Catalyzed Enantioselective Intermolecular Carboaminations via C-H Functionalizations. Angewandte Chemie (International Ed. in English). PMID 32986927 DOI: 10.1002/anie.202011140 |
0.428 |
|
2020 |
Woźniak Ł, Tan JF, Nguyen QH, Madron du Vigné A, Smal V, Cao YX, Cramer N. Catalytic Enantioselective Functionalizations of C-H Bonds by Chiral Iridium Complexes. Chemical Reviews. PMID 32897713 DOI: 10.1021/Acs.Chemrev.0C00559 |
0.534 |
|
2020 |
Cramer N, Mas-Roselló J, Herraiz AG, Audic B, Laverny A. Chiral cyclopentadienyl ligands: design, syntheses and applications in asymmetric catalysis. Angewandte Chemie (International Ed. in English). PMID 32672405 DOI: 10.1002/Anie.202008166 |
0.485 |
|
2020 |
Audic B, Cramer N. Rhodium(III)-Catalyzed Cyclopropane C-H/C-C Activation Sequence Provides Diastereoselective Access to α-Alkoxylated γ-Lactams. Organic Letters. 22: 5030-5034. PMID 32610918 DOI: 10.1021/Acs.Orglett.0C01606 |
0.435 |
|
2020 |
Wodrich MD, Ye B, Gonthier JF, Corminboeuf C, Cramer N. Corrigendum: Ligand-Controlled Regio-divergent Pathways of Rhodium(III)-Catalyzed Dihydroisoquinolone Synthesis - Experimental and Computational Studies of Different Cyclopentadienyls. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 7727. PMID 32557865 DOI: 10.1002/Chem.202001781 |
0.393 |
|
2020 |
Cramer N, Braconi E. A Chiral Naphthyridine Diimine Ligand Platform Enables Nickel-Catalyzed Asymmetric Alkylidenecyclopropanations. Angewandte Chemie (International Ed. in English). PMID 32521105 DOI: 10.1002/Anie.202006082 |
0.558 |
|
2020 |
Mas-Roselló J, Smejkal T, Cramer N. Iridium-catalyzed acid-assisted asymmetric hydrogenation of oximes to hydroxylamines. Science (New York, N.Y.). 368: 1098-1102. PMID 32499437 DOI: 10.1126/Science.Abb2559 |
0.49 |
|
2020 |
Cramer N, Duchemin C. Enantioselective CpxRhIII-Catalyzed Carboaminations of Acrylates. Angewandte Chemie (International Ed. in English). PMID 32410313 DOI: 10.1002/Ange.202006149 |
0.547 |
|
2020 |
Diesel J, Cramer N. Modular Chiral -Heterocyclic Carbene Ligands for the Nickel-Catalyzed Enantioselective C-H Functionalization of Heterocycles. Chimia. 74: 278-284. PMID 32331547 DOI: 10.2533/Chimia.2020.278 |
0.532 |
|
2020 |
Nguyen QH, Guo SM, Royal T, Baudoin O, Cramer N. Intermolecular Palladium(0)-Catalyzed Atropo-enantioselective C-H Arylation of Heteroarenes. Journal of the American Chemical Society. PMID 31967802 DOI: 10.1021/Jacs.9B12299 |
0.5 |
|
2020 |
Tan J, Bormann CT, Severin K, Cramer N. Alkynyl Triazenes as Fluoroalkyne Surrogates: Regioselective Access to 4-Fluoro-2-pyridones by a Rh(III)-Catalyzed C–H Activation–Lossen Rearrangement–Wallach Reaction Acs Catalysis. 10: 3790-3796. DOI: 10.1021/Acscatal.0C00499 |
0.433 |
|
2020 |
Reed JH, Cramer N. 1,3,2‐Diazaphospholenes Catalyze the Conjugate Reduction of Substituted Acrylic Acids Chemcatchem. 12: 4262-4266. DOI: 10.1002/Cctc.202000662 |
0.379 |
|
2019 |
Cramer N, Wang SG, Lui Y. Asymmetric Alkenyl C-H Functionalization by CpxRhIII forms 2H-Pyrrol-2-ones by [4+1]-Annulation of Acryl Amides and Allenes. Angewandte Chemie (International Ed. in English). PMID 31553519 DOI: 10.1002/Anie.201909971 |
0.492 |
|
2019 |
Tan JF, Bormann CT, Perrin FG, Chadwick FM, Severin K, Cramer N. Divergent Synthesis of Densely Substituted Arenes and Pyridines via Cyclotrimerization Reactions of Alkynyl Triazenes. Journal of the American Chemical Society. PMID 31244170 DOI: 10.1021/Jacs.9B04111 |
0.529 |
|
2019 |
Diesel J, Grosheva D, Kodama S, Cramer N. A Bulky Chiral N-Heterocyclic Carbene Nickel Catalyst Enables Enantioselective C-H Functionalizations of Indoles and Pyrroles. Angewandte Chemie (International Ed. in English). PMID 31095857 DOI: 10.1002/Anie.201904774 |
0.581 |
|
2019 |
Brauns M, Cramer N. Efficient Kinetic Resolution of Sulfur-Stereogenic Sulfoximines Exploiting CpXRh(III)-Catalyzed C-H Functionalization Marcus Brauns and Nicolai Cramer. Angewandte Chemie (International Ed. in English). PMID 31045299 DOI: 10.1002/Anie.201904543 |
0.532 |
|
2019 |
Reed JH, Donets PA, Miaskiewicz S, Cramer N. A 1,3,2-Diazaphospholene-Catalyzed Reductive Claisen Rearrangement. Angewandte Chemie (International Ed. in English). PMID 31044498 DOI: 10.1002/Anie.201904411 |
0.45 |
|
2019 |
Duchemin C, Cramer N. Chiral cyclopentadienyl Rh-catalyzed enantioselective cyclopropanation of electron-deficient olefins enable rapid access to UPF-648 and oxylipin natural products. Chemical Science. 10: 2773-2777. PMID 30996996 DOI: 10.1039/C8Sc05702H |
0.496 |
|
2019 |
Grosheva D, Cramer N. Exploitation of Unconventional Electrophiles in Enantioselective Pd(0)-Catalyzed C-H Functionalizations. Chimia. 73: 262-267. PMID 30975254 DOI: 10.2533/Chimia.2019.262 |
0.51 |
|
2019 |
Ozols K, Jang YS, Cramer N. Chiral Cyclopentadienyl Cobalt(III) Complexes Enable Highly Enantioselective 3d-Metal-Catalyzed C-H Functionalizations. Journal of the American Chemical Society. PMID 30901216 DOI: 10.1021/Jacs.9B02569 |
0.519 |
|
2019 |
Audic B, Wodrich MD, Cramer N. Mild complexation protocol for chiral CpRh and Ir complexes suitable for catalysis. Chemical Science. 10: 781-787. PMID 30774871 DOI: 10.1039/C8Sc04385J |
0.446 |
|
2019 |
Cramer N, Wang SG. An Enantioselective CpxRh(III)-Catalyzed C-H Functionalization / Ring-Opening Route to Chiral Cyclopentenylamines. Angewandte Chemie (International Ed. in English). PMID 30600903 DOI: 10.1002/Anie.201813953 |
0.541 |
|
2019 |
Duchemin C, Cramer N. One-step access to N-enoxyimides by gold-catalysed addition of N-hydroxyimides to terminal alkynes Organic Chemistry Frontiers. 6: 209-212. DOI: 10.1039/C8Qo01179F |
0.317 |
|
2019 |
Park SH, Wang S, Cramer N. Enantioselective Ruthenium(II)-Catalyzed Access to Benzonorcaradienes by Coupling of Oxabenzonorbornadienes and Alkynes Acs Catalysis. 9: 10226-10231. DOI: 10.1021/Acscatal.9B03858 |
0.514 |
|
2019 |
Diesel J, Cramer N. Generation of Heteroatom Stereocenters by Enantioselective C–H Functionalization Acs Catalysis. 9: 9164-9177. DOI: 10.1021/Acscatal.9B03194 |
0.459 |
|
2019 |
Duchemin C, Smits G, Cramer N. RhI, IrIII ,and CoIII Complexes with Atropchiral Biaryl Cyclopentadienyl Ligands: Syntheses, Structures, and Catalytic Activities Organometallics. 38: 3939-3947. DOI: 10.1021/Acs.Organomet.9B00365 |
0.466 |
|
2018 |
Cramer N, Sun Y. Enantioselective Access to S-Chiral 1,2-Benzothiazines by CpxRh(III) Catalyzed C-H Functionalization of Sulfoximines. Angewandte Chemie (International Ed. in English). PMID 30300950 DOI: 10.1002/Anie.201810887 |
0.534 |
|
2018 |
Cramer N, Grosheva D. Enantioselective Access to 1H-Isoindoles with Quaternary Stereogenic Centers by Pd(0) Catalyzed C-H Functionalization. Angewandte Chemie (International Ed. in English). PMID 30168246 DOI: 10.1002/Anie.201809173 |
0.484 |
|
2018 |
Cramer N, Jang YS, Wozniak L, Pedroni J. Access to P- and Axially-Chiral Biaryl Phosphine Oxides by Enantioselective CpxIrIII-Catalyzed C-H Arylations. Angewandte Chemie (International Ed. in English). PMID 30044513 DOI: 10.1002/Anie.201807749 |
0.52 |
|
2018 |
Cramer N, Newton CG, Braconi E, Kuziola J, Wodrich MD. Axially Chiral Dibenzazepinones via a Pd(0)-Catalyzed Atropo-enantioselective C-H Arylation. Angewandte Chemie (International Ed. in English). PMID 29963763 DOI: 10.1002/Anie.201806527 |
0.523 |
|
2018 |
Sun Y, Cramer N. Tailored trisubstituted chiral Cp Rh catalysts for kinetic resolutions of phosphinic amides. Chemical Science. 9: 2981-2985. PMID 29732080 DOI: 10.1039/C7Sc05411D |
0.489 |
|
2018 |
Diesel J, Finogenova AM, Cramer N. Nickel-Catalyzed Enantioselective Pyridone C-H Functionalizations Enabled by a Bulky N-Heterocyclic Carbene Ligand. Journal of the American Chemical Society. PMID 29543449 DOI: 10.1021/Jacs.8B01181 |
0.545 |
|
2018 |
Cramer N, Wang SG, Park SH. A Readily Accessible Class of Chiral Cp Ligands and their Application in Ru(II)-Catalyzed Enantioselective Syntheses of Dihydrobenzoindoles. Angewandte Chemie (International Ed. in English). PMID 29528173 DOI: 10.1002/Anie.201802244 |
0.453 |
|
2018 |
Cramer N, Miaskiewicz S, Reed JH, Donets PA, Oliveira CC. Chiral 1,3,2-Diazaphospholenes as Catalytic Molecular Hydrides for Enantioselective Conjugate Reductions. Angewandte Chemie (International Ed. in English). PMID 29461670 DOI: 10.1002/Anie.201801300 |
0.466 |
|
2017 |
Smits G, Audic B, Wodrich MD, Corminboeuf C, Cramer N. A β-Carbon elimination strategy for convenient access to cyclopentadienyl metal complexes. Chemical Science. 8: 7174-7179. PMID 29081949 DOI: 10.1039/C7Sc02986A |
0.361 |
|
2017 |
Cramer N, Jang YS, Dieckmann M. Cooperative Effects between Chiral CpxIrIII Catalysts and Chiral Carboxylic Acids in Enantioselective C-H Amidations of Phosphine Oxides. Angewandte Chemie (International Ed. in English). PMID 28941057 DOI: 10.1002/Anie.201708440 |
0.495 |
|
2017 |
Cramer N, Newton CG. One-step Multigram-scale Biomimetic Synthesis of Psiguadial B. Angewandte Chemie (International Ed. in English). PMID 28884886 DOI: 10.1002/Anie.201708333 |
0.449 |
|
2017 |
Pedroni J, Cramer N. Enantioselective C-H Functionalization-Addition Sequence Delivers Densely Substituted 3-Azabicyclo[3.1.0]hexanes. Journal of the American Chemical Society. PMID 28832139 DOI: 10.1021/Jacs.7B07024 |
0.5 |
|
2017 |
Severin K, Kossler D, Perrin F, Suleymanov A, Kiefer G, Scopelliti R, Cramer N. Divergent Asymmetric Synthesis of Polycyclic Compounds via Vinyl Triazenes. Angewandte Chemie (International Ed. in English). PMID 28696574 DOI: 10.1002/Anie.201706013 |
0.516 |
|
2017 |
Kossler D, Cramer N. Neutral chiral cyclopentadienyl Ru(ii)Cl catalysts enable enantioselective [2+2]-cycloadditions. Chemical Science. 8: 1862-1866. PMID 28553476 DOI: 10.1039/C6Sc05092A |
0.457 |
|
2017 |
Kossler D, Cramer N. Chiral Cyclopentadienyl Ruthenium Complexes as Versatile Catalysts for Enantioselective Transformations. Chimia. 71: 186-189. PMID 28446333 DOI: 10.2533/Chimia.2017.186 |
0.467 |
|
2017 |
Newton CG, Wang SG, Oliveira CC, Cramer N. Catalytic Enantioselective Transformations Involving C-H Bond Cleavage by Transition-Metal Complexes. Chemical Reviews. PMID 28212007 DOI: 10.1021/Acs.Chemrev.6B00692 |
0.446 |
|
2017 |
Grosheva D, Cramer N. Ketene Aminal Phosphates: Competent Substrates for Enantioselective Pd(0)-Catalyzed C–H Functionalizations Acs Catalysis. 7: 7417-7420. DOI: 10.1021/Acscatal.7B02783 |
0.404 |
|
2016 |
Sun Y, Cramer N. Rhodium(III)-Catalyzed Enantiotopic C-H Activation Enables Access to P-Chiral Cyclic Phosphinamides. Angewandte Chemie (International Ed. in English). PMID 27572545 DOI: 10.1002/Anie.201606637 |
0.484 |
|
2016 |
Ahlin JS, Cramer N. Chiral N-Heterocyclic Carbene Ligand Enabled Nickel(0)-Catalyzed Enantioselective Three-Component Couplings as Direct Access to Silylated Indanols. Organic Letters. PMID 27326716 DOI: 10.1021/Acs.Orglett.6B01492 |
0.518 |
|
2016 |
Heinz C, Cramer N. Total Synthesis of Fijiolide A. Chimia. 70: 258-62. PMID 27131110 DOI: 10.2533/Chimia.2016.258 |
0.392 |
|
2016 |
Pedroni J, Cramer N. 2-(Trifluoromethyl)indoles via Pd(0)-Catalyzed C(sp(3))-H Functionalization of Trifluoroacetimidoyl Chlorides. Organic Letters. PMID 27054603 DOI: 10.1021/Acs.Orglett.6B00795 |
0.413 |
|
2016 |
Newton CG, Kossler D, Cramer N. Asymmetric Catalysis Powered by Chiral Cyclopentadienyl Ligands. Journal of the American Chemical Society. PMID 26863546 DOI: 10.1021/Jacs.5B12964 |
0.431 |
|
2016 |
Pham MV, Cramer N. Enantioselective Access to Spirocyclic Sultams by Chiral Cp(x) -Rhodium(III)-Catalyzed Annulations. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 2270-3. PMID 26836575 DOI: 10.1002/Chem.201504998 |
0.513 |
|
2016 |
Cramer N. Designer Anhydride Clears the Path for Alkoxycarbonylations in Catellani Reactions Chem. 1: 522-523. DOI: 10.1016/J.Chempr.2016.09.014 |
0.413 |
|
2015 |
Souillart L, Cramer N. Enantioselective Rhodium-catalyzed C-C Bond Activation of Cyclobutanones. Chimia. 69: 187-90. PMID 26668935 DOI: 10.2533/Chimia.2015.187 |
0.501 |
|
2015 |
Pedroni J, Cramer N. TADDOL-based phosphorus(iii)-ligands in enantioselective Pd(0)-catalysed C-H functionalisations. Chemical Communications (Cambridge, England). PMID 26511604 DOI: 10.1039/C5Cc07929B |
0.445 |
|
2015 |
Kossler D, Cramer N. Chiral Cationic Cp(x)Ru(II) Complexes for Enantioselective Yne-Enone Cyclizations. Journal of the American Chemical Society. PMID 26374282 DOI: 10.1021/Jacs.5B08232 |
0.475 |
|
2015 |
Dieckmann M, Jang YS, Cramer N. Chiral Cyclopentadienyl Iridium(III) Complexes Promote Enantioselective Cycloisomerizations Giving Fused Cyclopropanes. Angewandte Chemie (International Ed. in English). PMID 26310394 DOI: 10.1002/Anie.201506483 |
0.441 |
|
2015 |
Heinz C, Cramer N. Synthesis of Fijiolide A via an Atropselective Paracyclophane Formation. Journal of the American Chemical Society. 137: 11278-81. PMID 26301726 DOI: 10.1021/Jacs.5B07964 |
0.434 |
|
2015 |
Pedroni J, Cramer N. Chiral γ-Lactams by Enantioselective Palladium(0)-Catalyzed Cyclopropane Functionalizations. Angewandte Chemie (International Ed. in English). 54: 11826-9. PMID 26271618 DOI: 10.1002/Anie.201505916 |
0.562 |
|
2015 |
Souillart L, Cramer N. Catalytic C-C Bond Activations via Oxidative Addition to Transition Metals. Chemical Reviews. PMID 26044343 DOI: 10.1021/Acs.Chemrev.5B00138 |
0.457 |
|
2015 |
Ye B, Cramer N. Chiral Cyclopentadienyls: Enabling Ligands for Asymmetric Rh(III)-Catalyzed C-H Functionalizations. Accounts of Chemical Research. 48: 1308-18. PMID 25884306 DOI: 10.1021/Acs.Accounts.5B00092 |
0.563 |
|
2015 |
Souillart L, Cramer N. Regiodivergent cyclobutanone cleavage: switching selectivity with different Lewis acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 1863-7. PMID 25476844 DOI: 10.1002/Chem.201406135 |
0.397 |
|
2015 |
Donets PA, Cramer N. Ligand-controlled regiodivergent nickel-catalyzed annulation of pyridones. Angewandte Chemie (International Ed. in English). 54: 633-7. PMID 25378295 DOI: 10.1002/Anie.201409669 |
0.482 |
|
2015 |
Souillart L, Cramer N. Enantioselective rhodium-catalyzed C-C bond activation of cyclobutanones Chimia. 69: 187-190. DOI: 10.2533/chimia.2015.187 |
0.301 |
|
2015 |
Ye B, Cramer N. Chiral Cyclopentadienyl Ligands Enable a Rhodium(III)-Catalyzed Enantioselective Access to Hydroxychromanes and Phthalides Synlett. 26: 1490-1495. DOI: 10.1055/S-0034-1380765 |
0.515 |
|
2015 |
Pedroni J, Saget T, Donets PA, Cramer N. Enantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system Chemical Science. 6: 5164-5171. DOI: 10.1039/C5Sc01909E |
0.533 |
|
2014 |
Pham MV, Cramer N. Rhodium(III)/copper(II)-promoted trans-selective heteroaryl acyloxylation of alkynes: stereodefined access to trans-enol esters. Angewandte Chemie (International Ed. in English). 53: 14575-9. PMID 25366553 DOI: 10.1002/Anie.201409450 |
0.474 |
|
2014 |
Wodrich MD, Ye B, Gonthier JF, Corminboeuf C, Cramer N. Ligand-controlled regiodivergent pathways of rhodium(III)-catalyzed dihydroisoquinolone synthesis: experimental and computational studies of different cyclopentadienyl ligands. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 15409-18. PMID 25283798 DOI: 10.1002/Chem.201404515 |
0.464 |
|
2014 |
Ahlin JS, Donets PA, Cramer N. Nickel(0)-catalyzed enantioselective annulations of alkynes and arylenoates enabled by a chiral NHC ligand: efficient access to cyclopentenones. Angewandte Chemie (International Ed. in English). 53: 13229-33. PMID 25258104 DOI: 10.1002/Anie.201408364 |
0.557 |
|
2014 |
Souillart L, Cramer N. Highly enantioselective rhodium(I)-catalyzed carbonyl carboacylations initiated by C-C bond activation. Angewandte Chemie (International Ed. in English). 53: 9640-4. PMID 25044652 DOI: 10.1002/Anie.201405834 |
0.511 |
|
2014 |
Pedroni J, Boghi M, Saget T, Cramer N. Access to β-lactams by enantioselective palladium(0)-catalyzed C(sp3)-H alkylation. Angewandte Chemie (International Ed. in English). 53: 9064-7. PMID 24986088 DOI: 10.1002/Anie.201405508 |
0.497 |
|
2014 |
Ye B, Cramer N. Asymmetric synthesis of isoindolones by chiral cyclopentadienyl-rhodium(III)-catalyzed C-H functionalizations. Angewandte Chemie (International Ed. in English). 53: 7896-9. PMID 24916401 DOI: 10.1002/Anie.201404895 |
0.579 |
|
2014 |
Tran DN, Cramer N. Biomimetic synthesis of (+)-ledene, (+)-viridiflorol, (-)-palustrol, (+)-spathulenol, and psiguadial A, C, and D via the platform terpene (+)-bicyclogermacrene. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 10654-60. PMID 24867775 DOI: 10.1002/Chem.201403082 |
0.394 |
|
2014 |
Pham MV, Cramer N. Aromatic homologation by non-chelate-assisted Rh(III)-catalyzed C-H functionalization of arenes with alkynes. Angewandte Chemie (International Ed. in English). 53: 3484-7. PMID 24554591 DOI: 10.1002/Anie.201310723 |
0.508 |
|
2014 |
Souillart L, Parker E, Cramer N. Asymmetric transformations via C-C bond cleavage. Topics in Current Chemistry. 346: 163-93. PMID 24531752 DOI: 10.1007/128_2013_505 |
0.427 |
|
2014 |
Souillart L, Parker E, Cramer N. Highly enantioselective rhodium(I)-catalyzed activation of enantiotopic cyclobutanone C-C bonds. Angewandte Chemie (International Ed. in English). 53: 3001-5. PMID 24519918 DOI: 10.1002/Anie.201311009 |
0.487 |
|
2014 |
Ye B, Donets PA, Cramer N. Chiral Cp-rhodium(III)-catalyzed asymmetric hydroarylations of 1,1-disubstituted alkenes. Angewandte Chemie (International Ed. in English). 53: 507-11. PMID 24311026 DOI: 10.1002/Anie.201309207 |
0.564 |
|
2014 |
Saget T, Cramer N. Enantioselective palladium(0)-catalyzed C-H arylation strategy for chiral heterocycles Pure and Applied Chemistry. 86: 265-272. DOI: 10.1515/Pac-2014-5029 |
0.53 |
|
2014 |
Souillart L, Cramer N. Exploitation of Rh(i)-Rh(iii) cycles in enantioselective C-C bond cleavages: Access to β-tetralones and benzobicyclo[2.2.2]octanones Chemical Science. 5: 837-840. DOI: 10.1039/C3Sc52753K |
0.435 |
|
2014 |
Parker E, Cramer N. Asymmetric Rhodium(I)-catalyzed C-C activations with zwitterionic bis-phospholane ligands Organometallics. 33: 780-787. DOI: 10.1021/Om4011627 |
0.501 |
|
2014 |
Pham MV, Cramer N. ChemInform Abstract: Aromatic Homologation by Non-Chelate-Assisted RhIII-Catalyzed C-H Functionalization of Arenes with Alkynes. Cheminform. 45: no-no. DOI: 10.1002/chin.201436104 |
0.346 |
|
2014 |
Trost BM, Bringley DA, Zhang T, Cramer N. ChemInform Abstract: Rapid Access to Spirocyclic Oxindole Alkaloids: Application of the Asymmetric Palladium-Catalyzed [3 + 2] Trimethylenemethane Cycloaddition. Cheminform. 45: no-no. DOI: 10.1002/chin.201420083 |
0.574 |
|
2014 |
Su Y, Straathof NJW, Hessel V, Noël T, More S, Bhosale R, Mateo-Alonso A, Fermi A, Ceroni P, Roy M, Gingras M, Bergamini G, Vione D, Minella M, Maurino V, ... ... Cramer N, et al. Cover Picture: Photochemical Transformations Accelerated in Continuous-Flow Reactors: Basic Concepts and Applications / Low-LUMO Pyrene-Fused Azaacenes / Synthesis, Characterization, and Metal Ion Coordination of a Multichromophoric Highly Luminescent Pol Chemistry - a European Journal. 20: 10529-10529. DOI: 10.1002/Chem.201490142 |
0.302 |
|
2013 |
Trost BM, Bringley DA, Zhang T, Cramer N. Rapid access to spirocyclic oxindole alkaloids: application of the asymmetric palladium-catalyzed [3 + 2] trimethylenemethane cycloaddition. Journal of the American Chemical Society. 135: 16720-35. PMID 24083654 DOI: 10.1021/Ja409013M |
0.655 |
|
2013 |
Tran DN, Cramer N. Rhodium-catalyzed dynamic kinetic asymmetric transformations of racemic allenes by the [3+2] annulation of aryl ketimines. Angewandte Chemie (International Ed. in English). 52: 10630-4. PMID 23956126 DOI: 10.1002/Anie.201304919 |
0.507 |
|
2013 |
Donets PA, Cramer N. Diaminophosphine oxide ligand enabled asymmetric nickel-catalyzed hydrocarbamoylations of alkenes. Journal of the American Chemical Society. 135: 11772-5. PMID 23909575 DOI: 10.1021/Ja406730T |
0.47 |
|
2013 |
Saget T, Cramer N. Enantioselective C-H arylation strategy for functionalized dibenzazepinones with quaternary stereocenters. Angewandte Chemie (International Ed. in English). 52: 7865-8. PMID 23784692 DOI: 10.1002/Anie.201303816 |
0.547 |
|
2013 |
Saget T, Perez D, Cramer N. Synthesis of functionalized spiroindolines via palladium-catalyzed methine C-H arylation. Organic Letters. 15: 1354-7. PMID 23452056 DOI: 10.1021/Ol400380Y |
0.492 |
|
2013 |
Ye B, Cramer N. A tunable class of chiral Cp ligands for enantioselective rhodium(III)-catalyzed C-H allylations of benzamides. Journal of the American Chemical Society. 135: 636-9. PMID 23286204 DOI: 10.1021/Ja311956K |
0.509 |
|
2012 |
Cramer N. Teaching enantioselectivity to C-H bond functionalizations: initial steps of a rather long shot. Chimia. 66: 869-72. PMID 23394245 DOI: 10.2533/Chimia.2012.869 |
0.455 |
|
2012 |
Saget T, Cramer N. Palladium(0)-catalyzed enantioselective C-H arylation of cyclopropanes: efficient access to functionalized tetrahydroquinolines. Angewandte Chemie (International Ed. in English). 51: 12842-5. PMID 23161777 DOI: 10.1002/Anie.201207959 |
0.457 |
|
2012 |
Ye B, Cramer N. Chiral cyclopentadienyl ligands as stereocontrolling element in asymmetric C-H functionalization. Science (New York, N.Y.). 338: 504-6. PMID 23112328 DOI: 10.1126/Science.1226938 |
0.502 |
|
2012 |
Pham MV, Ye B, Cramer N. Access to sultams by rhodium(III)-catalyzed directed C-H activation. Angewandte Chemie (International Ed. in English). 51: 10610-4. PMID 23002028 DOI: 10.1002/Anie.201206191 |
0.495 |
|
2012 |
Saget T, Cramer N. Heteroatom nucleophile induced C-C fragmentations to access functionalized allenes. Chimia. 66: 205-7. PMID 22613150 DOI: 10.2533/Chimia.2012.205 |
0.419 |
|
2012 |
Saget T, Lemouzy SJ, Cramer N. Chiral monodentate phosphines and bulky carboxylic acids: cooperative effects in palladium-catalyzed enantioselective C(sp3)-H functionalization. Angewandte Chemie (International Ed. in English). 51: 2238-42. PMID 22308174 DOI: 10.1002/Anie.201108511 |
0.488 |
|
2012 |
Donets PA, Saget T, Cramer N. Chiral monodentate trialkylphosphines based on the phospholane architecture Organometallics. 31: 8040-8046. DOI: 10.1021/Om3008772 |
0.526 |
|
2012 |
Saget T, Lemouzy SJ, Cramer N. Chirale einzähnige Phosphine und sperrige Carbonsäuren: kooperative Effekte in Pd-katalysierten enantioselektiven C(sp3)-H-Funktionalisierungen Angewandte Chemie. 124: 2281-2285. DOI: 10.1002/Ange.201108511 |
0.367 |
|
2011 |
Tran DN, Cramer N. Highly Selective Rhodium Catalyzed Domino C-H Activation/Cyclizations. Chimia. 65: 271-273. PMID 28982408 DOI: 10.2533/Chimia.2011.271 |
0.508 |
|
2011 |
Cramer N. Catalytic asymmetric functionalization of inert bonds and synthesis of bioactive natural products. Chimia. 65: 656-8. PMID 22026173 DOI: 10.2533/Chimia.2011.656 |
0.419 |
|
2011 |
Tran DN, Cramer N. Enantioselective rhodium(I)-catalyzed [3+2] annulations of aromatic ketimines induced by directed C-H activations. Angewandte Chemie (International Ed. in English). 50: 11098-102. PMID 21976453 DOI: 10.1002/Anie.201105766 |
0.539 |
|
2011 |
Seiser T, Saget T, Tran DN, Cramer N. Cyclobutanes in catalysis. Angewandte Chemie (International Ed. in English). 50: 7740-52. PMID 21793133 DOI: 10.1002/Anie.201101053 |
0.445 |
|
2011 |
Trans DN, Cramer N. Highly selective rhodium catalyzed domino C-H activation/cyclizations. Chimia. 65: 271-3. PMID 21678778 DOI: 10.2533/chimia.2011.271 |
0.419 |
|
2011 |
Waibel M, Cramer N. Desymmetrizations of meso-tert-norbornenols by rhodium(I)-catalyzed enantioselective retro-allylations. Chemical Communications (Cambridge, England). 47: 346-8. PMID 20820518 DOI: 10.1039/C0Cc01950J |
0.471 |
|
2011 |
Saget T, Cramer N. Convenient preparation of tri-tert-butylphosphonium tetrafluoroborate Synthesis. 2369-2371. DOI: 10.1055/S-0030-1260113 |
0.408 |
|
2011 |
Cramer N, Seiser T. β-carbon elimination from cyclobutanols: A clean access to alkylrhodium intermediates bearing a quaternary stereogenic center Synlett. 449-460. DOI: 10.1055/S-0030-1259536 |
0.467 |
|
2010 |
Seiser T, Cramer N. Enantioselective rhodium-catalyzed C-C bond activations. Chimia. 64: 153-6. PMID 21140909 DOI: 10.2533/Chimia.2010.153 |
0.466 |
|
2010 |
Seiser T, Cramer N. Rhodium(I)-catalyzed 1,4-silicon shift of unactivated silanes from aryl to alkyl: enantioselective synthesis of indanol derivatives. Angewandte Chemie (International Ed. in English). 49: 10163-7. PMID 21125550 DOI: 10.1002/Anie.201005399 |
0.415 |
|
2010 |
Saget T, Cramer N. Heteroatom-nucleophile-induced C-C fragmentations: synthesis of allenes and entry to domino reactions. Angewandte Chemie (International Ed. in English). 49: 8962-5. PMID 20927794 DOI: 10.1002/Anie.201004795 |
0.486 |
|
2010 |
Tran DN, Cramer N. syn-Selective rhodium(I)-catalyzed allylations of ketimines proceeding through a directed C-H activation/allene addition sequence. Angewandte Chemie (International Ed. in English). 49: 8181-4. PMID 20865713 DOI: 10.1002/Anie.201004179 |
0.508 |
|
2010 |
Waibel M, Cramer N. Palladium-catalyzed arylative ring-opening reactions of norbornenols: entry to highly substituted cyclohexenes, quinolines, and tetrahydroquinolines. Angewandte Chemie (International Ed. in English). 49: 4455-8. PMID 20480483 DOI: 10.1002/Anie.201001752 |
0.504 |
|
2010 |
Tran ND, Albicker M, Schneider L, Cramer N. Enantioselective assembly of the benzo[d]xanthene tetracyclic core of anti-influenza active natural products. Organic & Biomolecular Chemistry. 8: 1781-4. PMID 20449479 DOI: 10.1039/C002011G |
0.322 |
|
2010 |
Seiser T, Cramer N. Rhodium-catalyzed C-C bond cleavage: construction of acyclic methyl substituted quaternary stereogenic centers. Journal of the American Chemical Society. 132: 5340-1. PMID 20345153 DOI: 10.1021/Ja101469T |
0.491 |
|
2010 |
Seiser T, Cramer N. Rhodium(I)-catalyzed enantioselective activation of cyclobutanols: formation of cyclohexane derivatives with quaternary stereogenic centers. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3383-91. PMID 20146275 DOI: 10.1002/Chem.200903225 |
0.533 |
|
2010 |
Cramer N, Tran D. Rhodium-Catalyzed Domino C-H Activation-Intramolecular Allylation of Imines Synfacts. 2011: 0065-0065. DOI: 10.1055/s-0030-1259167 |
0.366 |
|
2010 |
Seiser T, Cathomen G, Cramer N. Enantioselective construction of indanones from cyclobutanols using a rhodium-catalyzed C-C/C-H/C-C bond activation process Synlett. 1699-1703. DOI: 10.1055/S-0029-1219959 |
0.395 |
|
2010 |
Saget T, Cramer N. Durch Heteroatom-Nukleophile induzierte C-C-Fragmentierungen: Synthese von Allenen und Ausgangspunkt für Dominoreaktionen Angewandte Chemie. 122: 9146-9149. DOI: 10.1002/Ange.201004795 |
0.328 |
|
2010 |
Trost BM, Cramer N, Silverman SM. Enantioselective construction of spirocyclic oxindolic cyclopentanes by palladium-catalyzed trimethylenemethane [3 + 2] cycloaddition Chemtracts. 23: 66-68. |
0.736 |
|
2009 |
Albicker MR, Cramer N. Enantioselective palladium-catalyzed direct arylations at ambient temperature: access to indanes with quaternary stereocenters. Angewandte Chemie (International Ed. in English). 48: 9139-42. PMID 19859927 DOI: 10.1002/Anie.200905060 |
0.433 |
|
2009 |
Seiser T, Roth OA, Cramer N. Enantioselective synthesis of indanols from tert-cyclobutanols using a rhodium-catalyzed C-C/C-H activation sequence. Angewandte Chemie (International Ed. in English). 48: 6320-3. PMID 19610009 DOI: 10.1002/Anie.200903189 |
0.434 |
|
2009 |
Seiser T, Cramer N. Enantioselective metal-catalyzed activation of strained rings. Organic & Biomolecular Chemistry. 7: 2835-40. PMID 19582290 DOI: 10.1039/B904405A |
0.402 |
|
2009 |
Cramer N, Waser J. The 44th euchems conference on stereochemistry (bürgenstock conference 2009) brunnen, may 17-22, 2009 Chimia. 63: 512-515. DOI: 10.2533/Chimia.2009.512 |
0.457 |
|
2008 |
Seiser T, Cramer N. Enantioselective C-C bond activation of allenyl cyclobutanes: access to cyclohexenones with quaternary stereogenic centers. Angewandte Chemie (International Ed. in English). 47: 9294-7. PMID 18972485 DOI: 10.1002/Anie.200804281 |
0.484 |
|
2008 |
Cramer N, Helbig S, Baro A, Laschat S, Diestel R, Sasse F, Mathieu D, Richter C, Kummerlöwe G, Luy B, Schwalbe H. Synthesis and biological properties of cylindramide derivatives: evidence for calcium-dependent cytotoxicity of tetramic acid lactams. Chembiochem : a European Journal of Chemical Biology. 9: 2474-86. PMID 18798209 DOI: 10.1002/Cbic.200800284 |
0.341 |
|
2008 |
Seiser T, Kamena F, Cramer N. Synthesis and biological activity of largazole and derivatives. Angewandte Chemie (International Ed. in English). 47: 6483-5. PMID 18633950 DOI: 10.1002/Anie.200802043 |
0.4 |
|
2008 |
Trost BM, Cramer N, Silverman SM. Palladium-Catalyzed Synthesis of Spirocyclic Cyclopentanes Synfacts. 2008: 73-73. DOI: 10.1055/S-2007-991428 |
0.635 |
|
2008 |
Trost BM, Cramer N, Silverman SM. ChemInform Abstract: Enantioselective Construction of Spirocyclic Oxindolic Cyclopentanes by Palladium-Catalyzed Trimethylenemethane-[3 + 2]-Cycloaddition. Cheminform. 39. DOI: 10.1002/chin.200807094 |
0.73 |
|
2008 |
Seiser T, Cramer N. Enantioselektive C-C-Bindungsaktivierung von Allenylcyclobutanen: Synthese von Cyclohexenonen mit quartären Stereozentren Angewandte Chemie. 120: 9435-9438. DOI: 10.1002/Ange.200804281 |
0.324 |
|
2008 |
Seiser T, Kamena F, Cramer N. Synthese und biologische Aktivität von Largazol und Derivaten Angewandte Chemie. 120: 6583-6585. DOI: 10.1002/Ange.200802043 |
0.317 |
|
2007 |
Trost BM, Cramer N, Silverman SM. Enantioselective construction of spirocyclic oxindolic cyclopentanes by palladium-catalyzed trimethylenemethane-[3+2]-cycloaddition. Journal of the American Chemical Society. 129: 12396-7. PMID 17880222 DOI: 10.1021/Ja075335W |
0.755 |
|
2007 |
Trost BM, Cramer N, Bernsmann H. Concise total synthesis of (+/-)-marcfortine B. Journal of the American Chemical Society. 129: 3086-7. PMID 17315880 DOI: 10.1021/Ja070142U |
0.567 |
|
2007 |
Trost BM, Cramer N, Bernsmann H. Synthesis of (±)-Marcfortine B Synfacts. 2007: 793-793. DOI: 10.1055/S-2007-968715 |
0.457 |
|
2007 |
Heibig S, Sauer S, Cramer N, Laschat S, Baro A, Frey W. Chiral bicyclo[3.3.0]octa-2,5-dienes as steering ligands in substrate-dependent rhodium-catalyzed 1,4-addition of arylboronic acids to enones Advanced Synthesis and Catalysis. 349: 2331-2337. DOI: 10.1002/Adsc.200700232 |
0.337 |
|
2006 |
Cramer N, Buchweitz M, Laschat S, Frey W, Baro A, Mathieu D, Richter C, Schwalbe H. Total synthesis and NMR investigations of cylindramide. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 2488-503. PMID 16389623 DOI: 10.1002/Chem.200501274 |
0.516 |
|
2006 |
Laschat S, Cramer N, Buchweitz M, Frey W, Baro A, Mathieu D, Richter C, Schwalbe H. Synthesis of Cylindramide Synfacts. 2006: 0986-0986. DOI: 10.1055/S-2006-949335 |
0.402 |
|
2006 |
Cramer N, Laschat S, Baro A. Chiral phosphites and phosphoramidites based on the tropane skeleton and their application in catalysis Organometallics. 25: 2284-2291. DOI: 10.1021/Om0510066 |
0.323 |
|
2005 |
Cramer N, Laschat S, Baro A, Schwalbe H, Richter C. Enantioselective total synthesis of cylindramide. Angewandte Chemie (International Ed. in English). 44: 820-2. PMID 15624223 DOI: 10.1002/Anie.200461823 |
0.476 |
|
2004 |
Cramer N, Juretschke J, Laschat S, Baro A, Frey W. Acid-promoted retro-Mannich reaction of N-protected tropenones to 2-substituted pyrroles European Journal of Organic Chemistry. 1397-1400. DOI: 10.1002/Ejoc.200300804 |
0.391 |
|
2003 |
Cramer N, Laschat S, Baro A, Frey W. Enantioselective Desymmetrization of Tropinone Derivatives by Hydroboration Synlett. 2175-2177. DOI: 10.1055/S-2003-42080 |
0.473 |
|
2003 |
Cramer N, Laschat S, Baro A. Enzymatic Resolution of Tropinone Derivatives Synlett. 2178-2181. DOI: 10.1055/S-2003-42079 |
0.415 |
|
Show low-probability matches. |