Volume 31, Issue 7
Preparative Organic Chemistry
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ChemInform Abstract: Ring-Opening Iodo- and Bromosilation of Cyclic Ethers by Treatment with Iodo- and Bromotrialkylsilane Equivalents.

Joji Ohshita

Joji Ohshita

Dep. Appl. Chem., Fac. Eng., Hiroshima Univ., Higashi-Hiroshima 739, Japan

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Arihiro Iwata

Arihiro Iwata

Dep. Appl. Chem., Fac. Eng., Hiroshima Univ., Higashi-Hiroshima 739, Japan

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Fujio Kanetani

Fujio Kanetani

Dep. Appl. Chem., Fac. Eng., Hiroshima Univ., Higashi-Hiroshima 739, Japan

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Atsutaka Kunai

Atsutaka Kunai

Dep. Appl. Chem., Fac. Eng., Hiroshima Univ., Higashi-Hiroshima 739, Japan

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Yasushi Yamamoto

Yasushi Yamamoto

Dep. Appl. Chem., Fac. Eng., Hiroshima Univ., Higashi-Hiroshima 739, Japan

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Chinami Matui

Chinami Matui

Dep. Appl. Chem., Fac. Eng., Hiroshima Univ., Higashi-Hiroshima 739, Japan

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First published: 10 June 2010

Abstract

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ChemInform Abstract

The ring-opening halosilation of five- and six-membered cyclic ethers using 1:2 mixtures of Et2NTms/alkyl halogenide (MeI, EtI, EtBr, AllylBr), or 1:1 mixtures of silane (Et3SiH, PhSi(Me)2H, Ph2Si(Me)H) and alkyl halogenide (MeI, AllylBr) in the presence of catalytic amount of palladium catalyst affords bifunctional halo(siloxy)alkanes, including halogenated silyl enol ethers.

chemical structure image

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