Design, Generation, and Characterization of a 1,5-Hexadiene Bearing Two Lophyl Radicals as a Probe of the Stepwise Mechanism for the Cope Rearrangement-Reference-Cited by-同舟云学术

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Design, Generation, and Characterization of a 1,5-Hexadiene Bearing Two Lophyl Radicals as a Probe of the Stepwise Mechanism for the Cope Rearrangement

Published:2011-05-15 Issue:5 Volume:84 Page:537-543
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ikeda Hiroshi,Matsuo Kazuki,Matsui Yasunori,Matsuoka Masaya,Mizuno Kazuhiko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference58 articles.

1. The Introduction of Substituted Vinyl Groups. V. A Rearrangement Involving the Migration of an Allyl Group in a Three-Carbon System1

2. The overlap of two allyl radicals or a four-centered transition state in the cope rearrangement

3. Kinetics of the cope rearrangement of 1,1-dideuteriohexa-1,5-diene

4. A frustrated Cope rearrangement: thermal interconversion of 2,6-diphenylhepta-1,6-diene and 1,5-diphenylbicyclo[3.2.0]heptane

5. The Conservation of Orbital Symmetry

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1. Photo-controllable room-temperature phosphorescence of organic photochromic polymers based on hexaarylbiimidazole;Science China Chemistry;2021-05-21

2. The development of carbon–carbon bond forming reactions of aminal radicals;Tetrahedron;2015-03

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