Please use this identifier to cite or link to this item:
|Title:||Highly enantioselective and regioselective substitution of morita-baylis-hillman carbonates with nitroalkanes|
|Citation:||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|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Mar 14, 2019
WEB OF SCIENCETM
checked on Mar 5, 2019
checked on Jan 12, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.