π-Facial Selectivity in the Diels–Alder Reaction of 5-Substituted 1,3-Cyclopentadienes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/11/66_11_3430/_pdf
Reference32 articles.
1. Orbital mixing rule
2. Modeling chemical reactivity. 5. Facial selectivity in Diels-Alder cycloadditions
3. .sigma./.pi. Interaction as a controlling factor in the stereoselectivity of addition reactions
4. Modeling of steric control of facial stereoselectivity. Diels-Alder cycloadditions of unsymmetrically substituted cyclopentadienes
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1. Hyperconjugative Aromaticity and Antiaromaticity Control the Reactivities and π-Facial Stereoselectivities of 5-Substituted Cyclopentadiene Diels–Alder Cycloadditions;The Journal of Organic Chemistry;2018-11-05
2. Synthesis of 7-norbornenols via Diels–Alder cycloadditions of cyclopentadienol generated by decomposition of ferrocenium cation;Tetrahedron Letters;2015-10
3. Complete Facial Selectivity in the Diels–Alder Reaction of a 5-Amino-5-carboxycyclopentadiene Derivative;Organic Letters;2011-05-26
4. Origins of the diastereoselectivity in hydrogen bonding directed Diels–Alder reactions of chiral dienes with achiral dienophiles: a computational study;Organic & Biomolecular Chemistry;2011
5. ChemInform Abstract: π-Facial Selectivity in the Diels-Alder Reaction of 5-Substituted 1, 3-Cyclopentadienes.;ChemInform;2010-08-19
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