Modulation of .pi.-facial selectivity in Diels-Alder cycloaddition to isodicyclopentafulvenes by remote para substitution of an exocyclic phenyl group
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00243a054
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Formation of Alkenes by Diels-Alder Reactions;Comprehensive Organic Transformations;2018-02-28
2. Facial Selectivity in the Diels-Alder Reactions of 2,2-Disubstituted Cyclopent-4-ene-1,3-dione Derivatives and a Computational Examination of the Facial Selectivity of the Diels-Alder Reactions of Structurally Related Dienes and Dienophiles;European Journal of Organic Chemistry;2011-12-28
3. Chemistry of pyramidalized alkenes;Tetrahedron;2005-05
4. 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,;The Journal of Organic Chemistry;2002-01-23
5. Structural Effects of C6 Substitution in 6-(4-(Dimethylamino)phenyl)fulvenes;The Journal of Organic Chemistry;1999-11-13
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