Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/75436
Title: A highly stereoselective synthesis of β-trifluoromethylated homoallylic alcohols in water
Authors: Loh, T.-P. 
Li, X.-R. 
Keywords: aldehydes
allylation
fluorine
indium
tin
Issue Date: 1997
Source: Loh, T.-P.,Li, X.-R. (1997). A highly stereoselective synthesis of β-trifluoromethylated homoallylic alcohols in water. Angewandte Chemie - International Edition in English 36 (9) : 980-982. ScholarBank@NUS Repository.
Abstract: A tin-mediated, indium trichloride promoted allylation reaction provided β-trifluoromethylated homoallylic alcohols, the building blocks of biologically active substances, in high yields and excellent stereoselectivity. Since the syntheses can be carried out in water, the reactive OH groups do not need to be protected, and even compounds that are insoluble in organic solvents can be used.
Source Title: Angewandte Chemie - International Edition in English
URI: http://scholarbank.nus.edu.sg/handle/10635/75436
ISSN: 05700833
Appears in Collections:Staff Publications

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