Highly Stereoselective Hydroxy-Directed Diels−Alder Reaction
Author:
Affiliation:
1. Department of Chemistry, 10 Marie Curie, University of Ottawa, Ottawa, Canada, K1N 6N5
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo020664m
Reference50 articles.
1. The Diels-Alder Reaction in Total Synthesis
2. Heteroatom Influence on the π-Facial Selectivity of Diels−Alder Cycloadditions to 1-Oxa-4-thia-6-vinylspiro[4.5]dec-6-ene, 3-Methoxy-3-methyl-2-vinylcyclohexene, and 3-Methoxy-2-vinylcyclohexene,
3. Diels−Alder Reactions of 5-Alkyl-1,3-cyclopentadienes
4. Facial Selectivity in the Diels−Alder Reactions of 5-Chloro-, 5-Bromo-, and 5-Iodo-1,3-cyclopentadiene and Derivatives
5. Diels−Alder Reactions of Chiral 1,3-Dienes
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