Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol202555v
Title: Highly enantioselective and regioselective substitution of morita-baylis-hillman carbonates with nitroalkanes
Authors: Chen, G.-Y.
Zhong, F.
Lu, Y. 
Issue Date: 18-Nov-2011
Source: Chen, G.-Y., Zhong, F., Lu, Y. (2011-11-18). Highly enantioselective and regioselective substitution of morita-baylis-hillman carbonates with nitroalkanes. Organic Letters 13 (22) : 6070-6073. ScholarBank@NUS Repository. https://doi.org/10.1021/ol202555v
Abstract: A highly enantioselective and regioselective substitution reaction of the Morita-Baylis-Hillman (MBH) carbonates with nitroalkanes catalyzed by a quinidine-derived tertiary amine-thiourea catalyst has been developed. The described method, which is different from most organocatalytic allylic substitutions of the MBH adducts to date, represents a novel approach to regioselectively functionalize the MBH adducts. © 2011 American Chemical Society.
Source Title: Organic Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/76304
ISSN: 15237060
DOI: 10.1021/ol202555v
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