1.3.4. transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide

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ID: 191958
2015
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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tian*2015communications1.3.4. Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Yingying Xu, Wugai An, Wenchao Ding, Haijian Liu, Laijin Tian*
Journal nanoscale research letters
Year 2015
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