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Trends in Organic Chemistry   Volumes    Volume 1 
Abstract
Convenient radical α-monoallylations of carbonyl compounds: Pentadienylation, methallylation, crotylation, and prenylation
Takeshi Toru, Tetsuo Yoneda, Tatsuya Okumura, Yoshihiko Watanabe, Yoshio Ueno
Pages: 43 - 52
Number of pages: 10
Trends in Organic Chemistry
Volume 1 

Copyright © 1990 Research Trends. All rights reserved

ABSTRACT
 
Free radical allylations of α-seleno carbonyl compounds with tributyl-2,4-pentadienyltin, -β-methallyltin, -crotyltin, and -prenyltin, are described. Such successful C-C bond formations, in particular with the crotyltin and the prenyltin, are owing to the high reactivity of the α-carbon radical, generated from α-seleno carbonyl compounds, toward allylic tin compounds. These reactions provide a powerful, convenient and efficient method for α-monoallylation of carbonyl compounds.
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