1.3.4. transesterification reaction of 2-methoxycarbonylethyldichlorotin hydroxide
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ID: 191958
2015
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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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tian*2015communications1.3.4.
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| Authors | ;Yingying Xu, Wugai An, Wenchao Ding, Haijian Liu, Laijin Tian* |
| Journal | nanoscale research letters |
| Year | 2015 |
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