1,2-Distannylation and -disilylation of cyclic allenes

K Kwetkat; B H Riches; J M Rosset; D J Brecknell; K Byriel; C H L Kennard; David James Young; U Schneider; T N Mitchell; W Kitching

doi:10.1039/CC9960000773

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1,2-Distannylation and -disilylation of cyclic allenes

Journal article

Peer reviewed

1,2-Distannylation and -disilylation of cyclic allenes

K Kwetkat, B H Riches, J M Rosset, D J Brecknell, K Byriel, C H L Kennard, David James Young, U Schneider, T N Mitchell and W Kitching

Chemical Communications, Vol.6, pp.773-774

1996

DOI: https://doi.org/10.1039/CC9960000773

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Abstract

cyclic allenes

Cyclo-1,2-dienes (C9-C13) are converted into the synthetically promising 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.

Details

Title: 1,2-Distannylation and -disilylation of cyclic allenes
Authors: K Kwetkat (Author)
B H Riches (Author)
J M Rosset (Author)
D J Brecknell (Author)
K Byriel (Author)
C H L Kennard (Author)
David James Young (Author)
U Schneider (Author)
T N Mitchell (Author)
W Kitching (Author)
Publication details: Chemical Communications, Vol.6, pp.773-774
Publisher: Royal Society of Chemistry (R S C) Publications
Date published: 1996
DOI: 10.1039/CC9960000773
ISSN: 1359-7345
Organisation Unit: University of the Sunshine Coast, Queensland
Language: English
Record Identifier: 99449113802621
Output Type: Journal article

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