A highly efficient radical clock as a probe of the mechanism of sulfone halogenation by perhaloalkanes-Reference-Cited by-同舟云学术

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A highly efficient radical clock as a probe of the mechanism of sulfone halogenation by perhaloalkanes

Published:1985-01 Issue:42 Volume:26 Page:5129-5130
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Vacher Bernard,Samat André,Chanon Michel

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. X-philic reactions

2. Vacher, B.; Samat, A.; Chanon, M. Tetrahedron Lett. (submitted for publication).

3. (endo)-5-(2-haloethyl)-2-norbornene. A new radical probe.

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1. The Regiochemistry of Cyclization of α-Sulfenyl-, α-Sulfinyl-, and α-Sulfonyl-5-hexenyl Radicals: Procedures Leading to Regioselective Syntheses of Cyclic Sulfones and Sulfoxides;The Journal of Organic Chemistry;2004-05-01

2. Ab Initio Study of Stereo- and Regioselectivity in the Diels−Alder Reaction between 2-Phenylcyclopentadiene and α-(Methylthio)acrylonitrile;The Journal of Organic Chemistry;1997-03-01

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