Reversible allylstannation of carbonyl compounds; a new route to mixed allyltins via allylcarbinols
V Peruzzo, G Tagliavini
Index: Peruzzo,V.; Tagliavini,G. Journal of Organometallic Chemistry, 1978 , vol. 162, p. 37 - 44
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Citation Number: 35
Abstract
Di-n-butylallyltin chloride readily adds to ketones and aldehydes to form organotin alkoxides of the type: n-Bu 2 ClSnOCR′R (CH 2 CHCH 2 ). In some cases this reaction is reversible. Thus, under suitable conditions, alkoxides of the type: n-Bu 2 XSnOCMeR(CH 2 CHCH 2 ) (X n-Bu, Cl; R Me, i-Pr, i-Bu, t-Bu), obtained by transalkoxylation reactions, furnish ketones and mixed allyltins, n-Bu 2 YSn-(CH 2 CHCH 2 ) (Y n-Bu, CH 2 CHCH 2 , ...
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