Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis

An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsaturated δ-lactones is disclosed. Enantioselectivity control involving the relatively remote enal γ-carbon was achieved via Lewis acid [Sc(OTf)3 or combined Sc(OTf)3/Mg(OTf)2] and NHC cooperative cataly...

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Main Authors: Mo, Junming, Chen, Xingkuan, Chi, Robin Yonggui
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/97651
http://hdl.handle.net/10220/11248
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-976512020-03-07T12:31:27Z Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis Mo, Junming Chen, Xingkuan Chi, Robin Yonggui School of Physical and Mathematical Sciences An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsaturated δ-lactones is disclosed. Enantioselectivity control involving the relatively remote enal γ-carbon was achieved via Lewis acid [Sc(OTf)3 or combined Sc(OTf)3/Mg(OTf)2] and NHC cooperative catalysis. 2013-07-12T01:25:16Z 2019-12-06T19:44:57Z 2013-07-12T01:25:16Z 2019-12-06T19:44:57Z 2012 2012 Journal Article Mo, J., Chen, X., & Chi, Y. R. (2012). Oxidative γ-Addition of Enals to Trifluoromethyl Ketones: Enantioselectivity Control via Lewis Acid/N-Heterocyclic Carbene Cooperative Catalysis. Journal of the American Chemical Society, 134(21), 8810-8813. https://hdl.handle.net/10356/97651 http://hdl.handle.net/10220/11248 10.1021/ja303618z 173625 en Journal of the American chemical society © 2012 American Chemical Society.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsaturated δ-lactones is disclosed. Enantioselectivity control involving the relatively remote enal γ-carbon was achieved via Lewis acid [Sc(OTf)3 or combined Sc(OTf)3/Mg(OTf)2] and NHC cooperative catalysis.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Mo, Junming
Chen, Xingkuan
Chi, Robin Yonggui
format Article
author Mo, Junming
Chen, Xingkuan
Chi, Robin Yonggui
spellingShingle Mo, Junming
Chen, Xingkuan
Chi, Robin Yonggui
Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
author_sort Mo, Junming
title Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
title_short Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
title_full Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
title_fullStr Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
title_full_unstemmed Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
title_sort oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via lewis acid/n-heterocyclic carbene cooperative catalysis
publishDate 2013
url https://hdl.handle.net/10356/97651
http://hdl.handle.net/10220/11248
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