Issue 8, 1998
From the journal:

Chemical Communications

On the origin of 1,5-induction in tin(IV) halide-promoted reactions of 4-alkoxyalk-2-enylstannanes with aldehydes

Lindsay A. Hobson,   Mark A. Vincent  and  Eric J. Thomas  

Abstract

A combination of experiment and theory has identified both the allyltin trichlorides 3 (R2 = Bn, H) as key intermediates in tin(IV) chloride-promoted reactions of allylstannanes 1 (R2 = Bn, H) and the transition structures that are involved in their reactions with aldehydes.

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Article information

DOI
https://doi.org/10.1039/A800781K
Article type
Paper

Chem. Commun., 1998, 899-900

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On the origin of 1,5-induction in tin(IV) halide-promoted reactions of 4-alkoxyalk-2-enylstannanes with aldehydes

L. A. Hobson, M. A. Vincent and E. J. Thomas, Chem. Commun., 1998, 899 DOI: 10.1039/A800781K

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