Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines

A highly reactive, chemo- and enantioselective addition of diphenylphosphine to α,β-unsaturated imines catalyzed by a palladacycle has been developed, thus providing the access to a series of chiral tertiary enaminophosphines in high yields. A putative catalytic cycle has also been proposed.

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Main Authors: Pullarkat, Sumod A., Huang, Yinhua, Chew, Renta Jonathan, Li, Yongxin, Leung, Pak-Hing
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/96145
http://hdl.handle.net/10220/17050
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-961452020-03-07T12:37:07Z Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines Pullarkat, Sumod A. Huang, Yinhua Chew, Renta Jonathan Li, Yongxin Leung, Pak-Hing School of Physical and Mathematical Sciences A highly reactive, chemo- and enantioselective addition of diphenylphosphine to α,β-unsaturated imines catalyzed by a palladacycle has been developed, thus providing the access to a series of chiral tertiary enaminophosphines in high yields. A putative catalytic cycle has also been proposed. 2013-10-30T04:34:52Z 2019-12-06T19:26:19Z 2013-10-30T04:34:52Z 2019-12-06T19:26:19Z 2012 2012 Journal Article Huang, Y., Chew, R. J., Pullarkat, S. A., Li, Y., & Leung, P.-H. (2012). Asymmetric Synthesis of Enaminophosphines via Palladacycle-Catalyzed Addition of Ph 2 PH to α,β-Unsaturated Imines . The Journal of Organic Chemistry, 77(16), 6849-6854. https://hdl.handle.net/10356/96145 http://hdl.handle.net/10220/17050 10.1021/jo300893s en The journal of organic chemistry
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description A highly reactive, chemo- and enantioselective addition of diphenylphosphine to α,β-unsaturated imines catalyzed by a palladacycle has been developed, thus providing the access to a series of chiral tertiary enaminophosphines in high yields. A putative catalytic cycle has also been proposed.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Pullarkat, Sumod A.
Huang, Yinhua
Chew, Renta Jonathan
Li, Yongxin
Leung, Pak-Hing
format Article
author Pullarkat, Sumod A.
Huang, Yinhua
Chew, Renta Jonathan
Li, Yongxin
Leung, Pak-Hing
spellingShingle Pullarkat, Sumod A.
Huang, Yinhua
Chew, Renta Jonathan
Li, Yongxin
Leung, Pak-Hing
Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines
author_sort Pullarkat, Sumod A.
title Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines
title_short Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines
title_full Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines
title_fullStr Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines
title_full_unstemmed Asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of Ph2PH to α,β-unsaturated imines
title_sort asymmetric synthesis of enaminophosphines via palladacycle-catalyzed addition of ph2ph to α,β-unsaturated imines
publishDate 2013
url https://hdl.handle.net/10356/96145
http://hdl.handle.net/10220/17050
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