Origins of Stereoselectivity in Intramolecular Aldol Reactions Catalyzed by Cinchona Amines
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja513096x
Reference145 articles.
1. Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations
2. Enantioselective catalysis 98. Preparation of 9-amino(9-deoxy)cinchona alkaloids
3. Synthesis of 9-amino(9-deoxy)epi cinchona alkaloids, general chiral organocatalysts for the stereoselective functionalization of carbonyl compounds
4. si-Enantioface selectivity in (S)-proline-catalysed asymmetric annelation
5. Theoretical Studies of Stereoselectivities of Intramolecular Aldol Cyclizations Catalyzed by Amino Acids
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