Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts

The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with α,β-unsaturated imines.

Bibliographic Details
Main Authors: Hao, Lin, Du, Yu, Lv, Hui, Chen, Xingkuan, Jiang, Huishen, Shao, Yaling, Chi, Robin Yonggui
Other Authors: School of Physical and Mathematical Sciences
Format: Journal Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/97284
http://hdl.handle.net/10220/10637
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author Hao, Lin
Du, Yu
Lv, Hui
Chen, Xingkuan
Jiang, Huishen
Shao, Yaling
Chi, Robin Yonggui
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Hao, Lin
Du, Yu
Lv, Hui
Chen, Xingkuan
Jiang, Huishen
Shao, Yaling
Chi, Robin Yonggui
author_sort Hao, Lin
collection NTU
description The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with α,β-unsaturated imines.
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spelling ntu-10356/972842020-03-07T12:34:43Z Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts Hao, Lin Du, Yu Lv, Hui Chen, Xingkuan Jiang, Huishen Shao, Yaling Chi, Robin Yonggui School of Physical and Mathematical Sciences The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with α,β-unsaturated imines. 2013-06-25T06:40:51Z 2019-12-06T19:40:53Z 2013-06-25T06:40:51Z 2019-12-06T19:40:53Z 2012 2012 Journal Article Hao, L., Du, Y., Lv, H., Chen, X., Jiang, H., Shao, Y., et al. (2012). Enantioselective Activation of Stable Carboxylate Esters as Enolate Equivalents via N-Heterocyclic Carbene Catalysts. Organic Letters, 14(8), 2154-2157. 1523-7060 https://hdl.handle.net/10356/97284 http://hdl.handle.net/10220/10637 10.1021/ol300676w 164430 en Organic letters © 2012 American Chemical Society.
spellingShingle Hao, Lin
Du, Yu
Lv, Hui
Chen, Xingkuan
Jiang, Huishen
Shao, Yaling
Chi, Robin Yonggui
Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
title Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
title_full Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
title_fullStr Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
title_full_unstemmed Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
title_short Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
title_sort enantioselective activation of stable carboxylate esters as enolate equivalents via n heterocyclic carbene catalysts
url https://hdl.handle.net/10356/97284
http://hdl.handle.net/10220/10637
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