Chiral Bicyclic Lactams. A New Study on Facial Alkylation
Author:
Affiliation:
1. Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo960952g
Reference7 articles.
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2. Solvation-controlled diastereofacial selectivity in alkylations of bicyclic lactam enolates
3. Conversion of L-pyroglutamic acid to 4-alkyl-substituted L-prolines. The synthesis of trans-4-cyclohexyl-L-proline
4. Chiral quaternary carbon compounds. II. An asymmetric synthesis of (R) or (S)-4,4-dialkyl-2-cyclopentenones
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