Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles

© 2016 Elsevier Ltd A sonochemical method for the synthesis of 2-aminobenzimidazoles and 2-aminobenzoxazoles, as well as chiral aminooxazolines and a chiral substituted quinazolin-5-one is reported. Using the Ph 3 P–I 2 system in the presence of triethylamine as a desulfurization agent, monothiourea...

Full description

Saved in:

Bibliographic Details
Main Authors:	Phakhodee W., Duangkamol C., Wiriya N., Pattarawarapan M.
Format:	Journal
Published:	2017
Online Access:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994322327&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42233
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	Chiang Mai University

id	th-cmuir.6653943832-42233
record_format	dspace
spelling	th-cmuir.6653943832-422332017-09-28T04:25:58Z Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles Phakhodee W. Duangkamol C. Wiriya N. Pattarawarapan M. © 2016 Elsevier Ltd A sonochemical method for the synthesis of 2-aminobenzimidazoles and 2-aminobenzoxazoles, as well as chiral aminooxazolines and a chiral substituted quinazolin-5-one is reported. Using the Ph 3 P–I 2 system in the presence of triethylamine as a desulfurization agent, monothioureas prepared in situ from the reaction of bis-nucleophiles with isothiocyanates underwent rapid cyclization to afford a variety of N-heterocyclic compounds in good to excellent yields under mild conditions. 2017-09-28T04:25:58Z 2017-09-28T04:25:58Z 2016-01-01 Journal 00404039 2-s2.0-84994322327 10.1016/j.tetlet.2016.10.060 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994322327&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42233
institution	Chiang Mai University
building	Chiang Mai University Library
country	Thailand
collection	CMU Intellectual Repository
description	© 2016 Elsevier Ltd A sonochemical method for the synthesis of 2-aminobenzimidazoles and 2-aminobenzoxazoles, as well as chiral aminooxazolines and a chiral substituted quinazolin-5-one is reported. Using the Ph 3 P–I 2 system in the presence of triethylamine as a desulfurization agent, monothioureas prepared in situ from the reaction of bis-nucleophiles with isothiocyanates underwent rapid cyclization to afford a variety of N-heterocyclic compounds in good to excellent yields under mild conditions.
format	Journal
author	Phakhodee W. Duangkamol C. Wiriya N. Pattarawarapan M.
spellingShingle	Phakhodee W. Duangkamol C. Wiriya N. Pattarawarapan M. Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
author_facet	Phakhodee W. Duangkamol C. Wiriya N. Pattarawarapan M.
author_sort	Phakhodee W.
title	Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
title_short	Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
title_full	Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
title_fullStr	Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
title_full_unstemmed	Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
title_sort	ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
publishDate	2017
url	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994322327&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42233
_version_	1681422150366396416

Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles

Similar Items