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
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
URI: http://scholarbank.nus.edu.sg/handle/10635/76304
ISSN: 15237060
DOI: 10.1021/ol202555v
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

25
checked on Mar 14, 2019

WEB OF SCIENCETM
Citations

26
checked on Mar 5, 2019

Page view(s)

44
checked on Jan 12, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.