PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles

A metal-free promoted direct oxidative C–N bond coupling of quinoxalinones and azoles for the rapid and effective synthesis of potent pharmaceutical important 3-(azol-1-yl)quinoxalin-2-one has been developed. Employing PIDA as the easily available mediator, the desired coupling products were isolate...

Full description

Saved in:
Bibliographic Details
Main Authors: Watchara Wimonsong, Sirilata Yotphan
Other Authors: Mahidol University
Format: Article
Published: 2022
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/76280
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Mahidol University
id th-mahidol.76280
record_format dspace
spelling th-mahidol.762802022-08-04T18:23:04Z PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles Watchara Wimonsong Sirilata Yotphan Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics A metal-free promoted direct oxidative C–N bond coupling of quinoxalinones and azoles for the rapid and effective synthesis of potent pharmaceutical important 3-(azol-1-yl)quinoxalin-2-one has been developed. Employing PIDA as the easily available mediator, the desired coupling products were isolated in moderate to excellent yields with a good substrate scope under operational simplicity and mild reaction conditions. Preliminary mechanistic studies suggested that a radical process is likely to be involved in the reaction. 2022-08-04T08:12:00Z 2022-08-04T08:12:00Z 2021-02-12 Article Tetrahedron. Vol.81, (2021) 10.1016/j.tet.2020.131919 14645416 00404020 2-s2.0-85099636406 https://repository.li.mahidol.ac.th/handle/123456789/76280 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099636406&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Watchara Wimonsong
Sirilata Yotphan
PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
description A metal-free promoted direct oxidative C–N bond coupling of quinoxalinones and azoles for the rapid and effective synthesis of potent pharmaceutical important 3-(azol-1-yl)quinoxalin-2-one has been developed. Employing PIDA as the easily available mediator, the desired coupling products were isolated in moderate to excellent yields with a good substrate scope under operational simplicity and mild reaction conditions. Preliminary mechanistic studies suggested that a radical process is likely to be involved in the reaction.
author2 Mahidol University
author_facet Mahidol University
Watchara Wimonsong
Sirilata Yotphan
format Article
author Watchara Wimonsong
Sirilata Yotphan
author_sort Watchara Wimonsong
title PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
title_short PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
title_full PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
title_fullStr PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
title_full_unstemmed PIDA-induced oxidative C–N bond coupling of quinoxalinones and azoles
title_sort pida-induced oxidative c–n bond coupling of quinoxalinones and azoles
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/76280
_version_ 1763494297810763776