Volume 26, Issue 19
Preparative Organic Chemistry
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ChemInform Abstract: Stereoselective Synthesis of Di- and Trisubstituted Alkenes via Intermolecular Addition of Vinyl Radicals to Alkenes.

K. MIURA

K. MIURA

Dep. Chem., Univ. Tsukuba, Tsukuba, Ibaraki 305, Japan

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D. ITOH

D. ITOH

Dep. Chem., Univ. Tsukuba, Tsukuba, Ibaraki 305, Japan

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T. HONDO

T. HONDO

Dep. Chem., Univ. Tsukuba, Tsukuba, Ibaraki 305, Japan

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A. HOSOMI

A. HOSOMI

Dep. Chem., Univ. Tsukuba, Tsukuba, Ibaraki 305, Japan

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First published: May 9, 1995

Abstract

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ChemInform Abstract

Different vinyl iodides are treated with Bu3SnH in the presence of several electron-poor alkenes in order to get insight into the scope of the reaction. The E/Z ratio of the products does not depend on the temperature; however, the yields at 25 °C are much lower than that found at 80 °C. On the other hand, the stereoselectivity is largely dependent on the substitution pattern of the starting iodides.

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