Single and Double Diastereoselection in Azomethine Ylide Cycloaddition Reactions with Unsaturated Chiral Bicyclic Lactams
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/jo9600870
Reference39 articles.
1. The First Asymmetric 1,3-Dipolar Cycloaddition of 1-Methyl-3-oxidopyridinium and (R)s-p-Tolyl Vinyl Sulfoxide. An Enantioselective Synthesis of (1S)-(−)-2α-Tropanol
2. Diastereofacial selectivity in azomethine ylide cycloaddition reactions derived from chiral α-cyanoaminosilanes
3. Stereoselective 1,3-dipolar cycloadditions of photochemically generated azomethine ylides to Oppolzer's chiral acryloyl sultam. An asymmetric approach to quinocarcin
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