Exocyclic substituent effects in the unsymmetrically cycloadditions of electron-deficient heptafulvenes with electron-rich fulvenes: Stereoselectivity, periselectivity, and regioselectivity-Reference-Cited by-同舟云学术

Exocyclic substituent effects in the unsymmetrically cycloadditions of electron-deficient heptafulvenes with electron-rich fulvenes: Stereoselectivity, periselectivity, and regioselectivity

Published:1997-12 Issue:51 Volume:53 Page:17275-17296
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Liu Ching-Yang,Shie Huei-Yan,Chen Shin-Yi,You Chiung-Yi,Wang Wei-Chang,Hua Liang-Neng,Yang He-Jiun,Tseng Chih-Min

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Cycloadditions of electron-deficient 8,8-disubstituted heptafulvenes to electron-rich 6,6-disubstituted fulvenes

2. Steric effects in the cycloaddition reactions of electron-deficient unsymmetrically 8,8-disubstituted 8-cyano-8-(methoxycarbonyl)heptafulvene with electron-rich 6,6-diphenyl- and 6,6-dimethylfulvenes

3. Heterocycles by cycloaddition. Part 7. Cycloaddition reactions of mesoionic dithiolones with fulvenes

4. Reaktionen von Fulvenen mit 1,3-dipolaren Verbindungen, I Reaktionen von 6-Arylfulvenen mit 1,3-Oxazolium-5-olaten

5. Reaktionen von Fulvenen mit 1,3-dipolaren Verbindungen, II Reaktionen von 6,6-disubstituierten Fulvenen mit 3-Methyl-2,4-diphenyl-1,3-oxazolium-5-olat

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1. Expanding the Frontiers of Higher-Order Cycloadditions;Accounts of Chemical Research;2019-12-02

2. An overview of the cycloaddition chemistry of fulvenes and emerging applications;Beilstein Journal of Organic Chemistry;2019-09-06

3. Constructing Molecular Complexity and Diversity by Cycloaddition Reactions of Fulvenes;Cross Conjugation;2016-04-08

4. Catalytic Asymmetric [8+2] Cycloaddition for the Construction of Cycloheptatriene-Fused Pyrrolidin-3,3’-Oxindoles;Acta Chimica Sinica;2014

5. Catalytic Asymmetric [8+2] Cycloaddition: Synthesis of Cycloheptatriene-Fused Pyrrole Derivatives;Angewandte Chemie International Edition;2013-04-19