Year |
Citation |
Score |
2023 |
Maji R, Mallojjala SC, Wheeler SE. Electrostatic Interactions in Asymmetric Organocatalysis. Accounts of Chemical Research. PMID 37410532 DOI: 10.1021/acs.accounts.3c00198 |
0.622 |
|
2023 |
Maji R, Ghosh S, Grossmann O, Zhang P, Leutzsch M, Tsuji N, List B. A Catalytic Asymmetric Hydrolactonization. Journal of the American Chemical Society. PMID 37043821 DOI: 10.1021/jacs.3c01404 |
0.625 |
|
2022 |
Ouyang J, Maji R, Leutzsch M, Mitschke B, List B. Design of an Organocatalytic Asymmetric (4 + 3) Cycloaddition of 2-Indolylalcohols with Dienolsilanes. Journal of the American Chemical Society. PMID 35523203 DOI: 10.1021/jacs.2c02216 |
0.466 |
|
2022 |
Ghosh S, Erchinger JE, Maji R, List B. Catalytic Asymmetric Spirocyclizing Diels-Alder Reactions of Enones: Stereoselective Total and Formal Syntheses of α-Chamigrene, β-Chamigrene, Laurencenone C, Colletoic Acid, and Omphalic Acid. Journal of the American Chemical Society. 144: 6703-6708. PMID 35389217 DOI: 10.1021/jacs.2c01971 |
0.543 |
|
2021 |
List B, Grossmann O, Maji R, Aukland MH, Lee S. Catalytic Asymmetric Additions of Enol Silanes to in situ Generated Cyclic, Aliphatic N-Acyliminium Ions. Angewandte Chemie (International Ed. in English). PMID 34897932 DOI: 10.1002/anie.202115036 |
0.735 |
|
2021 |
Kennemur JL, Maji R, Scharf MJ, List B. Catalytic Asymmetric Hydroalkoxylation of C-C Multiple Bonds. Chemical Reviews. 121: 14649-14681. PMID 34860509 DOI: 10.1021/acs.chemrev.1c00620 |
0.443 |
|
2021 |
Díaz-Oviedo CD, Maji R, List B. The Catalytic Asymmetric Intermolecular Prins Reaction. Journal of the American Chemical Society. 143: 20598-20604. PMID 34846874 DOI: 10.1021/jacs.1c10245 |
0.599 |
|
2021 |
Amatov T, Tsuji N, Maji R, Schreyer L, Zhou H, Leutzsch M, List B. Confinement-Controlled, Either - or -Selective Catalytic Asymmetric Mukaiyama Aldolizations of Propionaldehyde Enolsilanes. Journal of the American Chemical Society. PMID 34436899 DOI: 10.1021/jacs.1c07447 |
0.611 |
|
2021 |
Zhu C, Mandrelli F, Zhou H, Maji R, List B. Catalytic Asymmetric Synthesis of Unprotected β-Amino Acids. Journal of the American Chemical Society. PMID 33645969 DOI: 10.1021/jacs.1c00249 |
0.544 |
|
2020 |
List B, Gerosa G, Schwengers S, De CK, Maji R. Homologation of the Fischer Indolization: A Quinoline Synthesis via Homo-Diaza-Cope Rearrangement *. Angewandte Chemie (International Ed. in English). PMID 32621795 DOI: 10.1002/Anie.202005798 |
0.558 |
|
2020 |
List B, Maji R. Proton-Coupled-Electron-Transfer-Mediated Enantioselective Hydroamination of Alkenes Synfacts. 16: 962. DOI: 10.1055/S-0040-01707432 |
0.413 |
|
2020 |
Gerosa GG, Schwengers SA, Maji R, De CK, List B. Homologisierung der Fischer‐Indol‐Synthese: Chinoline via Homo‐Diaza‐Cope‐Umlagerung Angewandte Chemie. DOI: 10.1002/Ange.202005798 |
0.374 |
|
2019 |
Maji R, Ugale H, Wheeler SE. Understanding the Reactivity and Selectivity of Fluxional Chiral DMAP-Catalyzed Kinetic Resolutions of Axially Chiral Biaryls. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30657217 DOI: 10.1002/Chem.201806068 |
0.729 |
|
2018 |
Maji R, Mallojjala SC, Wheeler SE. Chiral phosphoric acid catalysis: from numbers to insights. Chemical Society Reviews. PMID 29355873 DOI: 10.1039/C6Cs00475J |
0.611 |
|
2017 |
Maji R, Wheeler SE. Importance of Electrostatic Effects in the Stereoselectivity of NHC-Catalyzed Kinetic Resolutions. Journal of the American Chemical Society. PMID 28823166 DOI: 10.1021/Jacs.7B01796 |
0.732 |
|
2017 |
Maji R, Champagne PA, Houk KN, Wheeler SE. Activation Mode and Origin of Selectivity in Chiral Phosphoric Acid-Catalyzed Oxacycle Formation by Intramolecular Oxetane Desymmetrizations Acs Catalysis. 7: 7332-7339. DOI: 10.1021/Acscatal.7B02993 |
0.708 |
|
2013 |
Hajra S, Aziz SM, Maji R. Organocatalytic enantioselective conjugate addition of nitromethane to alkylidenemalonates: asymmetric synthesis of pyrrolidine-3-carboxylic acid derivatives Rsc Advances. 3: 10185. DOI: 10.1039/C3Ra42014K |
0.457 |
|
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