Metal-free amidation of carboxylic acids with tertiary amines

© 2016 The Royal Society of Chemistry. A direct amidation of carboxylic acids with tertiary amines could be carried out in the presence of the Ph3P-I2 activator. With an appropriate reagent addition sequence, a range of carboxylic acids including aliphatic, allylic, and aromatic acids could be conve...

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Main Authors:	Wong Phakhodee, Sirilak Wangngae, Mookda Pattarawarapan
Format:	Journal
Published:	2018
Subjects:	Chemical Engineering Chemistry
Online Access:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84976633635&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/55389
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Institution:	Chiang Mai University

id	th-cmuir.6653943832-55389
record_format	dspace
spelling	th-cmuir.6653943832-553892018-09-05T02:56:40Z Metal-free amidation of carboxylic acids with tertiary amines Wong Phakhodee Sirilak Wangngae Mookda Pattarawarapan Chemical Engineering Chemistry © 2016 The Royal Society of Chemistry. A direct amidation of carboxylic acids with tertiary amines could be carried out in the presence of the Ph3P-I2 activator. With an appropriate reagent addition sequence, a range of carboxylic acids including aliphatic, allylic, and aromatic acids could be converted into their corresponding tertiary amides under mild conditions without requirement of metal catalysis. 2018-09-05T02:55:07Z 2018-09-05T02:55:07Z 2016-01-01 Journal 20462069 2-s2.0-84976633635 10.1039/c6ra12801g https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84976633635&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/55389
institution	Chiang Mai University
building	Chiang Mai University Library
country	Thailand
collection	CMU Intellectual Repository
topic	Chemical Engineering Chemistry
spellingShingle	Chemical Engineering Chemistry Wong Phakhodee Sirilak Wangngae Mookda Pattarawarapan Metal-free amidation of carboxylic acids with tertiary amines
description	© 2016 The Royal Society of Chemistry. A direct amidation of carboxylic acids with tertiary amines could be carried out in the presence of the Ph3P-I2 activator. With an appropriate reagent addition sequence, a range of carboxylic acids including aliphatic, allylic, and aromatic acids could be converted into their corresponding tertiary amides under mild conditions without requirement of metal catalysis.
format	Journal
author	Wong Phakhodee Sirilak Wangngae Mookda Pattarawarapan
author_facet	Wong Phakhodee Sirilak Wangngae Mookda Pattarawarapan
author_sort	Wong Phakhodee
title	Metal-free amidation of carboxylic acids with tertiary amines
title_short	Metal-free amidation of carboxylic acids with tertiary amines
title_full	Metal-free amidation of carboxylic acids with tertiary amines
title_fullStr	Metal-free amidation of carboxylic acids with tertiary amines
title_full_unstemmed	Metal-free amidation of carboxylic acids with tertiary amines
title_sort	metal-free amidation of carboxylic acids with tertiary amines
publishDate	2018
url	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84976633635&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/55389
_version_	1681424496651665408

Metal-free amidation of carboxylic acids with tertiary amines

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