Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles

An enantioselective Michael addition reaction of diphenylphosphine to substituted alkenylisoxazoles has been developed. The reaction proceeds efficiently under mild conditions with high yields (up to 99%) and moderate to excellent enantioselectivities (up to 92%) thus providing a hitherto unavailabl...

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Main Authors: Chew, Renta Jonathan, Huang, Yinhua, Li, Yongxin, Pullarkat, Sumod A., Leung, Pak-Hing
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2014
Subjects:
Online Access:https://hdl.handle.net/10356/102819
http://hdl.handle.net/10220/19200
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1028192020-03-07T12:34:55Z Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles Chew, Renta Jonathan Huang, Yinhua Li, Yongxin Pullarkat, Sumod A. Leung, Pak-Hing School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry An enantioselective Michael addition reaction of diphenylphosphine to substituted alkenylisoxazoles has been developed. The reaction proceeds efficiently under mild conditions with high yields (up to 99%) and moderate to excellent enantioselectivities (up to 92%) thus providing a hitherto unavailable direct access to a library of chiral tertiary phosphine-functionalized isoxazoles. 2014-04-09T07:42:11Z 2019-12-06T21:00:44Z 2014-04-09T07:42:11Z 2019-12-06T21:00:44Z 2013 2013 Journal Article Chew, R. J., Huang, Y., Li, Y., Pullarkat, S. A., & Leung, P. H. (2013). Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles. Advanced Synthesis & Catalysis, 355(7), 1403-1408. 1615-4150 https://hdl.handle.net/10356/102819 http://hdl.handle.net/10220/19200 10.1002/adsc.201300164 en Advanced Synthesis & Catalysis © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Organic chemistry
spellingShingle DRNTU::Science::Chemistry::Organic chemistry
Chew, Renta Jonathan
Huang, Yinhua
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
description An enantioselective Michael addition reaction of diphenylphosphine to substituted alkenylisoxazoles has been developed. The reaction proceeds efficiently under mild conditions with high yields (up to 99%) and moderate to excellent enantioselectivities (up to 92%) thus providing a hitherto unavailable direct access to a library of chiral tertiary phosphine-functionalized isoxazoles.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Chew, Renta Jonathan
Huang, Yinhua
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
format Article
author Chew, Renta Jonathan
Huang, Yinhua
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
author_sort Chew, Renta Jonathan
title Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
title_short Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
title_full Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
title_fullStr Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
title_full_unstemmed Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
title_sort enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles
publishDate 2014
url https://hdl.handle.net/10356/102819
http://hdl.handle.net/10220/19200
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