Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine

© 2020 Georg Thieme Verlag. All rights reserved. A convenient ultrasound-assisted one-pot synthesis of N -acylcyanamides starting from readily available carboxylic acids and sodium cyanamide has been developed. Upon activation in the presence of trichloroisocyanuric acid (TCCA) and triphenylphosphin...

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Main Authors: Wong Phakhodee, Dolnapa Yamano, Mookda Pattarawarapan
Format: Journal
Published: 2020
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/70401
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-704012020-10-14T08:29:12Z Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine Wong Phakhodee Dolnapa Yamano Mookda Pattarawarapan Chemistry © 2020 Georg Thieme Verlag. All rights reserved. A convenient ultrasound-assisted one-pot synthesis of N -acylcyanamides starting from readily available carboxylic acids and sodium cyanamide has been developed. Upon activation in the presence of trichloroisocyanuric acid (TCCA) and triphenylphosphine, a range of carboxylic acids was converted into N -acylcyanamides in good to excellent yields within 10 minutes at room temperature without base. Remarkably, N -acyl-substituted imidazolones were readily accessible through guanylation-cyclization of the in situ generated N -acylcyanamides. 2020-10-14T08:29:12Z 2020-10-14T08:29:12Z 2020-04-22 Journal 14372096 09365214 2-s2.0-85082668479 10.1055/s-0039-1691583 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082668479&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/70401
institution Chiang Mai University
building Chiang Mai University Library
continent Asia
country Thailand
Thailand
content_provider Chiang Mai University Library
collection CMU Intellectual Repository
topic Chemistry
spellingShingle Chemistry
Wong Phakhodee
Dolnapa Yamano
Mookda Pattarawarapan
Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine
description © 2020 Georg Thieme Verlag. All rights reserved. A convenient ultrasound-assisted one-pot synthesis of N -acylcyanamides starting from readily available carboxylic acids and sodium cyanamide has been developed. Upon activation in the presence of trichloroisocyanuric acid (TCCA) and triphenylphosphine, a range of carboxylic acids was converted into N -acylcyanamides in good to excellent yields within 10 minutes at room temperature without base. Remarkably, N -acyl-substituted imidazolones were readily accessible through guanylation-cyclization of the in situ generated N -acylcyanamides.
format Journal
author Wong Phakhodee
Dolnapa Yamano
Mookda Pattarawarapan
author_facet Wong Phakhodee
Dolnapa Yamano
Mookda Pattarawarapan
author_sort Wong Phakhodee
title Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine
title_short Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine
title_full Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine
title_fullStr Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine
title_full_unstemmed Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine
title_sort ultrasound-assisted synthesis of n -acylcyanamides and n -acyl-substituted imidazolones from carboxylic acids by using trichloroisocyanuric acid/triphenylphosphine
publishDate 2020
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082668479&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/70401
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