Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands

We report herein the first examples of asymmetric Mizoroki–Heck reactions using benzyl electrophiles. A new phosphoramidite was identified to be an effective chiral ligand in the palladium–catalyzed reaction. The reaction is compatible with polar functional groups and can be readily scaled up. Sever...

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Main Authors: Yang, Zhigang, Zhou, Jianrong Steve
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/97595
http://hdl.handle.net/10220/11228
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-975952020-03-07T12:31:21Z Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands Yang, Zhigang Zhou, Jianrong Steve School of Physical and Mathematical Sciences We report herein the first examples of asymmetric Mizoroki–Heck reactions using benzyl electrophiles. A new phosphoramidite was identified to be an effective chiral ligand in the palladium–catalyzed reaction. The reaction is compatible with polar functional groups and can be readily scaled up. Several cyclic olefins worked well as olefin components. Thirty-one examples are included. 2013-07-11T07:56:18Z 2019-12-06T19:44:26Z 2013-07-11T07:56:18Z 2019-12-06T19:44:26Z 2012 2012 Journal Article Yang, Z., & Zhou, J. S. (2012). Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands. Journal of the American chemical society, 134(29), 11833-11835. https://hdl.handle.net/10356/97595 http://hdl.handle.net/10220/11228 10.1021/ja304099j 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 We report herein the first examples of asymmetric Mizoroki–Heck reactions using benzyl electrophiles. A new phosphoramidite was identified to be an effective chiral ligand in the palladium–catalyzed reaction. The reaction is compatible with polar functional groups and can be readily scaled up. Several cyclic olefins worked well as olefin components. Thirty-one examples are included.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Yang, Zhigang
Zhou, Jianrong Steve
format Article
author Yang, Zhigang
Zhou, Jianrong Steve
spellingShingle Yang, Zhigang
Zhou, Jianrong Steve
Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
author_sort Yang, Zhigang
title Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
title_short Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
title_full Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
title_fullStr Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
title_full_unstemmed Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
title_sort palladium-catalyzed, asymmetric mizoroki–heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands
publishDate 2013
url https://hdl.handle.net/10356/97595
http://hdl.handle.net/10220/11228
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