Stereochemical Aspects in the Asymmetric Michael Addition of Chiral Imines to Substituted Electrophilic Alkenes
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo960140k
Reference15 articles.
1. Reviews: (a) d'Angelo, J.; Desmaële, D.; Dumas, F.; Guingant, A.Tetrahedron: Asymmetry1992,3,459−505. (b) d'Angelo, J.; Cavé, C.; Desmaële, D.; Dumas, F.Trends inOrganic Synthesis;Pandalai, S. G., Ed.; Trivandrum: India, 1993; Vol. 4, pp 555−615.
2. The asymmetric Michael reaction using chiral imines under neutral conditions: Stereochemical evidences in support of a cyclic transition state
3. Geminate-substituted cyclopentadienes. 1. Synthesis of 5,5-dialkylcyclopentadienes via 4,4-dialkylcyclopent-2-en-1-ones
4. (b) Desmaële, D.; d'Angelo, J.; Bois, C.Tetrahedron: Asymmetry1990,1, 759−762.
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