1.3.4. transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide
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1.3.4. transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide

;Yingying Xu, Wugai An, Wenchao Ding, Haijian Liu, Laijin Tian*
nanoscale research letters 2015 Vol. 1 pp. -
153
tian*2015communications1.3.4.

Abstract

The title compound, CH3OCOCH2CH2SnCl2(OH) (1), readily undergotransesterification into the corresponding analogues, ROCOCH2CH2SnCl2(OH) (R = CH3CH2, 2; CH3CH2CH2, 3; CH2=CHCH2,4), when reacted with an alcohol ROH under reflux. The structural featuresof these compounds have been described, and the possible mechanismof the transesterification reaction has been suggested.

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sciencechemistryinorganic chemistry

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