Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles

Asymmetric arylation of alkylnitriles forms quaternary stereocenters in good enantiocontrol for the first time. A lithium heterodimer consisting of an alkylnitrile anion and a disilylamide ion is the actual species responsible for the stereodetermining transmetalation in the catalytic cycle.

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Main Authors: Jiao, Zhiwei, Chee, Kwok Wei, Zhou, Jianrong Steve
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2017
Subjects:
Online Access:https://hdl.handle.net/10356/84965
http://hdl.handle.net/10220/43605
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-849652023-02-28T19:29:53Z Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles Jiao, Zhiwei Chee, Kwok Wei Zhou, Jianrong Steve School of Physical and Mathematical Sciences Palladium catalysis Alkylnitrile Asymmetric arylation of alkylnitriles forms quaternary stereocenters in good enantiocontrol for the first time. A lithium heterodimer consisting of an alkylnitrile anion and a disilylamide ion is the actual species responsible for the stereodetermining transmetalation in the catalytic cycle. MOE (Min. of Education, S’pore) Accepted version 2017-08-18T01:15:52Z 2019-12-06T15:54:31Z 2017-08-18T01:15:52Z 2019-12-06T15:54:31Z 2016 Journal Article Jiao, Z., Chee, K. W., & Zhou, J. S. (2016). Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles. Journal of the American Chemical Society, 138(50), 16240-16243. 0002-7863 https://hdl.handle.net/10356/84965 http://hdl.handle.net/10220/43605 10.1021/jacs.6b11610 en Journal of the American Chemical Society © 2016 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of the American Chemical Society, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/jacs.6b11610]. 5 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Palladium catalysis
Alkylnitrile
spellingShingle Palladium catalysis
Alkylnitrile
Jiao, Zhiwei
Chee, Kwok Wei
Zhou, Jianrong Steve
Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles
description Asymmetric arylation of alkylnitriles forms quaternary stereocenters in good enantiocontrol for the first time. A lithium heterodimer consisting of an alkylnitrile anion and a disilylamide ion is the actual species responsible for the stereodetermining transmetalation in the catalytic cycle.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Jiao, Zhiwei
Chee, Kwok Wei
Zhou, Jianrong Steve
format Article
author Jiao, Zhiwei
Chee, Kwok Wei
Zhou, Jianrong Steve
author_sort Jiao, Zhiwei
title Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles
title_short Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles
title_full Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles
title_fullStr Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles
title_full_unstemmed Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles
title_sort palladium-catalyzed asymmetric α-arylation of alkylnitriles
publishDate 2017
url https://hdl.handle.net/10356/84965
http://hdl.handle.net/10220/43605
_version_ 1759855246962589696