Asymmetric Synthesis of a Constituent of Iris Essential Oil by Homoenolate Alkylation of a Chiral Bicyclic Lactam
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/jo9719214
Reference8 articles.
1. Chiral bicyclic Lactams as homoenolate equivalents: An asymmetric route to 5-substituted cyclohexenones
2. Etudes sur les matières végétales volatiles XC. Présence d' apocynine (acéto-vanillone) dans l'huile essentielle d'iris
3. Preparation of optically active cyclohexenones: Chirons for the lipophilic moiety of flowery- and woody-like odorant ketones
4. Preparation of functionalized ketones via low temperature grignard reaction
5. Facile regioselective formation of thiopeptide linkages from oligopeptides with new thionation reagents
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