The Mechanism of the Reaction of (Aryloxy)trimethylstannane with Benzyl Bromide giving Aryl Benzyl Ether
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/54/1/54_1_307/_pdf
Reference6 articles.
1. The reactions of trimethyl(methylthio)- and trialkyl(arylthio)stannanes with alkyl halides
2. Kinetic and Stereochemical Studies of the Reaction of Trialkyl(alkylthio and arylthio)stannanes with Haloalkanes
3. A kinetic study for the reaction of aryloxytrimethylsilane with methanesulfinyl chloride giving aryl methanesulfinate
4. STUDIES RELATING TO METHYL TIN DERIVATIVES. I. INTRODUCTION. II. ACTION OF ZINC ON TRIMETHYL TIN BROMIDE. III. TRIMETHYL TIN PHENOLATE. IV. DECAMETHYLSTANNOBUTANE
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4. Mechanism of the Reaction of (Arylthio)trimethylgermanes with 1-Aryl-1-bromoethanes—Kinetic and Stereochemical Studies—;Bulletin of the Chemical Society of Japan;1989-08
5. The Mechanism of the Reaction of (Aryloxy)trimethylstannane with Methanesulfonyl Chloride. Solvent and Substituent Effects on the Rate of the Reaction;Bulletin of the Chemical Society of Japan;1983-02
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