Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles

Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles

10.1002/anie.201307757

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Bibliographic Details
Main Authors: Wang, T., Yao, W., Zhong, F., Pang, G.H., Lu, Y.
Other Authors: CHEMISTRY
Format: Article
Published: 2014
Subjects:
γ-addition
allylation
bifunctional phosphines
oxindoles
quaternary carbon centers
Online Access:http://scholarbank.nus.edu.sg/handle/10635/94509
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Institution: National University of Singapore
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spelling sg-nus-scholar.10635-945092023-10-26T07:29:54Z Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles Wang, T. Yao, W. Zhong, F. Pang, G.H. Lu, Y. CHEMISTRY γ-addition allylation bifunctional phosphines oxindoles quaternary carbon centers 10.1002/anie.201307757 Angewandte Chemie - International Edition 53 11 2964-2968 ACIEF 2014-10-16T08:36:53Z 2014-10-16T08:36:53Z 2014-03-10 Article Wang, T., Yao, W., Zhong, F., Pang, G.H., Lu, Y. (2014-03-10). Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles. Angewandte Chemie - International Edition 53 (11) : 2964-2968. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.201307757 14337851 http://scholarbank.nus.edu.sg/handle/10635/94509 000336846300016 Scopus
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic γ-addition
allylation
bifunctional phosphines
oxindoles
quaternary carbon centers
spellingShingle γ-addition
allylation
bifunctional phosphines
oxindoles
quaternary carbon centers
Wang, T.
Yao, W.
Zhong, F.
Pang, G.H.
Lu, Y.
Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles
description 10.1002/anie.201307757
author2 CHEMISTRY
author_facet CHEMISTRY
Wang, T.
Yao, W.
Zhong, F.
Pang, G.H.
Lu, Y.
format Article
author Wang, T.
Yao, W.
Zhong, F.
Pang, G.H.
Lu, Y.
author_sort Wang, T.
title Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles
title_short Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles
title_full Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles
title_fullStr Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles
title_full_unstemmed Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: Use of prochiral nucleophiles
title_sort phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: use of prochiral nucleophiles
publishDate 2014
url http://scholarbank.nus.edu.sg/handle/10635/94509
_version_ 1781786112752091136

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