[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines

[Cp*RhCl2]2 catalyzes the formation of 1,2-dihydroquinolines from the reaction of two terminal alkynes and an aniline. This reaction is believed to proceed via an alkyne hydroamination followed by an alkyne insertion.

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Main Authors:	Kumaran, Elumalai, Leong, Weng Kee
Other Authors:	School of Physical and Mathematical Sciences
Format:	Article
Language:	English
Published:	2015
Subjects:	DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds
Online Access:	https://hdl.handle.net/10356/96389 http://hdl.handle.net/10220/38498
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Institution:	Nanyang Technological University
Language:	English

id	sg-ntu-dr.10356-96389
record_format	dspace
spelling	sg-ntu-dr.10356-963892023-02-28T19:40:14Z [CpRhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines Kumaran, Elumalai Leong, Weng Kee School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds [CpRhCl2]2 catalyzes the formation of 1,2-dihydroquinolines from the reaction of two terminal alkynes and an aniline. This reaction is believed to proceed via an alkyne hydroamination followed by an alkyne insertion. MOE (Min. of Education, S’pore) Accepted version 2015-08-24T02:17:21Z 2019-12-06T19:29:47Z 2015-08-24T02:17:21Z 2019-12-06T19:29:47Z 2015 2015 Journal Article Kumaran, E., & Leong, W. K. (2015). [Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines. Organometallics, 34(9), 1779-1782. https://hdl.handle.net/10356/96389 http://hdl.handle.net/10220/38498 10.1021/om501253v en Organometallics © 2015 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Organometallics, 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/om501253v]. 4 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	DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds
spellingShingle	DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds Kumaran, Elumalai Leong, Weng Kee [Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
description	[Cp*RhCl2]2 catalyzes the formation of 1,2-dihydroquinolines from the reaction of two terminal alkynes and an aniline. This reaction is believed to proceed via an alkyne hydroamination followed by an alkyne insertion.
author2	School of Physical and Mathematical Sciences
author_facet	School of Physical and Mathematical Sciences Kumaran, Elumalai Leong, Weng Kee
format	Article
author	Kumaran, Elumalai Leong, Weng Kee
author_sort	Kumaran, Elumalai
title	[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
title_short	[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
title_full	[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
title_fullStr	[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
title_full_unstemmed	[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
title_sort	[cp*rhcl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
publishDate	2015
url	https://hdl.handle.net/10356/96389 http://hdl.handle.net/10220/38498
_version_	1759856095929565184

[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines

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