Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers

10.1002/anie.201102094

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Main Authors:	Zhong, F., Han, X., Wang, Y., Lu, Y.
Other Authors:	CHEMISTRY
Format:	Article
Published:	2014
Subjects:	amino acids asymmetric synthesis cycloaddition phosphines spiro compounds
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/93943
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-939432024-11-08T19:34:48Z Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers Zhong, F. Han, X. Wang, Y. Lu, Y. CHEMISTRY amino acids asymmetric synthesis cycloaddition phosphines spiro compounds 10.1002/anie.201102094 Angewandte Chemie - International Edition 50 34 7837-7841 ACIEA 2014-10-16T08:30:16Z 2014-10-16T08:30:16Z 2011-08-16 Article Zhong, F., Han, X., Wang, Y., Lu, Y. (2011-08-16). Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers. Angewandte Chemie - International Edition 50 (34) : 7837-7841. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.201102094 14337851 http://scholarbank.nus.edu.sg/handle/10635/93943 000294175700019 Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	amino acids asymmetric synthesis cycloaddition phosphines spiro compounds
spellingShingle	amino acids asymmetric synthesis cycloaddition phosphines spiro compounds Zhong, F. Han, X. Wang, Y. Lu, Y. Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
description	10.1002/anie.201102094
author2	CHEMISTRY
author_facet	CHEMISTRY Zhong, F. Han, X. Wang, Y. Lu, Y.
format	Article
author	Zhong, F. Han, X. Wang, Y. Lu, Y.
author_sort	Zhong, F.
title	Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
title_short	Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
title_full	Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
title_fullStr	Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
title_full_unstemmed	Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
title_sort	highly enantioselective [3+2] annulation of morita-baylis-hillman adducts mediated by l-threonine-derived phosphines: synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers
publishDate	2014
url	http://scholarbank.nus.edu.sg/handle/10635/93943
_version_	1821181840093872128

Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: Synthesis of 3-spirocyclopentene-2- oxindoles having two contiguous quaternary centers

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