Enantioselective Benzoylation of α-Amino Esters Using (S)-1-Benzoyl-2- (α-acetoxyethyl)benzimidazole, a Chiral Benzimidazolide
Author:
Affiliation:
1. Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (E), Mumbai 400098, India avkarnik@chem.mu.ac.in
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo070962p
Reference37 articles.
1. Kinetic Resolutions of Indolines by a Nonenzymatic Acylation Catalyst
2. First example of chiral N-heterocyclic carbenes as catalysts for kinetic resolution
3. 3-(N,N-Diacylamino)quinazolin-4(3H)-ones as enantioselective acylating agents for amines
4. Kinetic resolution of amino alcohol derivatives with a chiral nucleophilic catalyst: access to enantiopure cyclic cis-amino alcoholsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b1/b108753c/
5. Asymmetric Catalysis with “Planar-Chiral” Derivatives of 4-(Dimethylamino)pyridine
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