Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4039(99)01976-0
Title: An enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane
Authors: Loh, T.-P. 
Zhou, J.-R.
Li, X.-R. 
Keywords: Allylation
Carbonyl
Enantioselectivity
Indium
Trifluoromethyl
Issue Date: 24-Dec-1999
Citation: Loh, T.-P., Zhou, J.-R., Li, X.-R. (1999-12-24). An enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane. Tetrahedron Letters 40 (52) : 9333-9336. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(99)01976-0
Abstract: An enantioselective indium-mediated addition reaction of allylic bromides to carbonyl compounds was achieved in dichloromethane in the presence of (-)-cinchonidine. The desired products were obtained in moderate to excellent yields and with up to 75% enantioselectivity.
Source Title: Tetrahedron Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/75563
ISSN: 00404039
DOI: 10.1016/S0040-4039(99)01976-0
Appears in Collections:Staff Publications

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