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,
Author:
Affiliation:
1. Department of Chemistry, Indian Institute of Technology, Kanpur 208 016, India, and Department of Chemistry, University of Calgary, Calgary, Alberta, Canada T2N 1N4
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0106400
Reference36 articles.
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2. Diels−Alder Reactions of 5-Alkyl-1,3-cyclopentadienes
3. Modulation of .pi.-facial selectivity in Diels-Alder cycloaddition to isodicyclopentafulvenes by remote para substitution of an exocyclic phenyl group
4. The “cieplak effect”: Hyperconjugative interactions in diels alder reactions.
5. Propellanes. XLVI. Steric and electronic effects as observed in reactions of propellanes
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