[Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles
[Cp∗IrCl2]2 catalyses the cyclization of 2-alkynylanilines into indoles. A wide variety of substrates is tolerated. A reaction pathway involving intramolecular hydroamination is proposed.
Saved in:
Main Authors: | , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2014
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/103623 http://hdl.handle.net/10220/24547 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-103623 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1036232023-02-28T19:44:41Z [Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles Kumaran, Elumalai Leong, Weng Kee School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds [Cp∗IrCl2]2 catalyses the cyclization of 2-alkynylanilines into indoles. A wide variety of substrates is tolerated. A reaction pathway involving intramolecular hydroamination is proposed. MOE (Min. of Education, S’pore) Accepted version 2014-12-26T06:31:12Z 2019-12-06T21:16:32Z 2014-12-26T06:31:12Z 2019-12-06T21:16:32Z 2014 2014 Journal Article Kumaran, E., & Leong, W. K. (2014). [Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles. Tetrahedron letters, 55(40), 5495-5498. 0040-4039 https://hdl.handle.net/10356/103623 http://hdl.handle.net/10220/24547 10.1016/j.tetlet.2014.08.053 en Tetrahedron letters © 2014 Elsevier B.V. This is the author created version of a work that has been peer reviewed and accepted for publication by Tetrahedron Letters, Elsevier B.V. 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/10.1016/j.tetlet.2014.08.053]. 10 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∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
description |
[Cp∗IrCl2]2 catalyses the cyclization of 2-alkynylanilines into indoles. A wide variety of substrates is tolerated. A reaction pathway involving intramolecular hydroamination is proposed. |
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∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
title_short |
[Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
title_full |
[Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
title_fullStr |
[Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
title_full_unstemmed |
[Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
title_sort |
[cp∗ircl2]2-catalysed cyclization of 2-alkynylanilines into indoles |
publishDate |
2014 |
url |
https://hdl.handle.net/10356/103623 http://hdl.handle.net/10220/24547 |
_version_ |
1759854075181006848 |