Issue 6, 1996
From the journal:

Chemical Communications

1,2-Distannylation and -disilylation of cyclic allenes

Klaus Kwetkat,   Bruce H. Riches,   Jean-Marie Rosset,   Douglas J. Brecknell,   Karl Byriel,   Colin H. L. Kennard,   David J. Young,   Ulrich Schneider,   Terence N. Mitchell  and  William Kitching  

Abstract

Cyclo-1,2-dienes(C9–C13) are converted into the synthetically promissing 2,3-bis(trimethylsilyl)- and 2,3-bis(trimethylstannyl)cycloalk-1-enes by disilylation with lithium chlorotrimethylsilane in tetrahydrofuran, and Pd0-catalysed addition of hexaalkyldistannes, respectively.

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Article information

DOI
https://doi.org/10.1039/CC9960000773
Article type
Paper

Chem. Commun., 1996, 773-774

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1,2-Distannylation and -disilylation of cyclic allenes

K. Kwetkat, B. H. Riches, J. Rosset, D. J. Brecknell, K. Byriel, C. H. L. Kennard, D. J. Young, U. Schneider, T. N. Mitchell and W. Kitching, Chem. Commun., 1996, 773 DOI: 10.1039/CC9960000773

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