Stereoselectivity in Diels–Alder reactions-Reference-Cited by-同舟云学术

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Stereoselectivity in Diels–Alder reactions

Published:1979-10-01 Issue:19 Volume:57 Page:2564-2568
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Kakushima Masatoshi

Abstract

Two competing effects, secondary attractive interactions and closed-shell repulsions, provide the main control of endo–exo stereoselectivity of Diels–Alder cycloadditions.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/v79-414

Cited by 36 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. Pericyclic Reactions;Organic Synthesis;2017

2. Catalysis of Diels-Alder Reactions in Water and in Hydrogen-Bonding Environments;PATAI'S Chemistry of Functional Groups;2009-12-15

3. Solvent-free Diels–Alder reactions of in situ generated cyclopentadiene;Green Chem.;2009

4. 1-Acetoxy-1,3-butadiene;Encyclopedia of Reagents for Organic Synthesis;2007-03-15

5. Simple preparation of cobaloxime dienyl complexes and their exo selective Diels–Alder cycloadducts;Journal of Organometallic Chemistry;2003-09

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