Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.

An efficient triflic acid-catalyzed Friedländer annulation of 2-aminobenzophenone and ketone to afford quinolines under microwave irradiation is reported herein. The methodology gives a variety of quinolines with moderate to high yields (30-90%), achieved with 5 mol% of the Brønsted acid.

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Bibliographic Details
Main Author:	Hoeng, Murni.
Other Authors:	Philip Wai Hong Chan
Format:	Final Year Project
Language:	English
Published:	2010
Subjects:	DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
Online Access:	http://hdl.handle.net/10356/39834
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Institution:	Nanyang Technological University
Language:	English

id	sg-ntu-dr.10356-39834
record_format	dspace
spelling	sg-ntu-dr.10356-398342023-02-28T23:17:04Z Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation. Hoeng, Murni. Philip Wai Hong Chan School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis An efficient triflic acid-catalyzed Friedländer annulation of 2-aminobenzophenone and ketone to afford quinolines under microwave irradiation is reported herein. The methodology gives a variety of quinolines with moderate to high yields (30-90%), achieved with 5 mol% of the Brønsted acid. Bachelor of Science in Chemistry and Biological Chemistry 2010-06-07T02:56:17Z 2010-06-07T02:56:17Z 2010 2010 Final Year Project (FYP) http://hdl.handle.net/10356/39834 en 28 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::Organic synthesis
spellingShingle	DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis Hoeng, Murni. Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
description	An efficient triflic acid-catalyzed Friedländer annulation of 2-aminobenzophenone and ketone to afford quinolines under microwave irradiation is reported herein. The methodology gives a variety of quinolines with moderate to high yields (30-90%), achieved with 5 mol% of the Brønsted acid.
author2	Philip Wai Hong Chan
author_facet	Philip Wai Hong Chan Hoeng, Murni.
format	Final Year Project
author	Hoeng, Murni.
author_sort	Hoeng, Murni.
title	Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
title_short	Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
title_full	Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
title_fullStr	Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
title_full_unstemmed	Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
title_sort	synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
publishDate	2010
url	http://hdl.handle.net/10356/39834
_version_	1759856917662924800

Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.

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