alpha-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and other N-heterocyclesviadecarboxylative oxidative annulation reaction
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Viji, Mayavan | - |
dc.contributor.author | Vishwanath, Manjunatha | - |
dc.contributor.author | Sim, Jaeuk | - |
dc.contributor.author | Park, Yunjeong | - |
dc.contributor.author | Jung, Chanhyun | - |
dc.contributor.author | Lee, Seohu | - |
dc.contributor.author | Lee, Heesoon | - |
dc.contributor.author | Lee, Kiho | - |
dc.contributor.author | Jung, Jae-Kyung | - |
dc.date.accessioned | 2021-08-30T10:54:15Z | - |
dc.date.available | 2021-08-30T10:54:15Z | - |
dc.date.created | 2021-06-19 | - |
dc.date.issued | 2020-10-11 | - |
dc.identifier.issn | 2046-2069 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/52467 | - |
dc.description.abstract | A metal-free and efficient procedure for the synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and indolo[1,2-a]quinoxaline has been developed. The key features of our method include thein situgeneration of aldehyde from alpha-hydroxy acid in the presence of TBHP (tert-butyl hydrogen peroxide), and further condensation with various amines, followed by intramolecular cyclization and subsequent oxidation to afford the corresponding quinoxalines, quinazolinones derivatives in moderate to high yields. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.subject | ONE-POT SYNTHESIS | - |
dc.subject | COPPER-CATALYZED SYNTHESIS | - |
dc.subject | 2,3-DISUBSTITUTED QUINAZOLIN-4(3H)-ONES | - |
dc.subject | ANTIMALARIAL ACTIVITY | - |
dc.subject | POTENTIAL INHIBITORS | - |
dc.subject | EFFICIENT SYNTHESIS | - |
dc.subject | PHENYLACETIC ACIDS | - |
dc.subject | BOND ACTIVATION | - |
dc.subject | DERIVATIVES | - |
dc.subject | CYCLIZATION | - |
dc.title | alpha-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and other N-heterocyclesviadecarboxylative oxidative annulation reaction | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Kiho | - |
dc.identifier.doi | 10.1039/d0ra07093a | - |
dc.identifier.scopusid | 2-s2.0-85093821555 | - |
dc.identifier.wosid | 000578727600029 | - |
dc.identifier.bibliographicCitation | RSC ADVANCES, v.10, no.61, pp.37202 - 37208 | - |
dc.relation.isPartOf | RSC ADVANCES | - |
dc.citation.title | RSC ADVANCES | - |
dc.citation.volume | 10 | - |
dc.citation.number | 61 | - |
dc.citation.startPage | 37202 | - |
dc.citation.endPage | 37208 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.subject.keywordPlus | ONE-POT SYNTHESIS | - |
dc.subject.keywordPlus | COPPER-CATALYZED SYNTHESIS | - |
dc.subject.keywordPlus | 2,3-DISUBSTITUTED QUINAZOLIN-4(3H)-ONES | - |
dc.subject.keywordPlus | ANTIMALARIAL ACTIVITY | - |
dc.subject.keywordPlus | POTENTIAL INHIBITORS | - |
dc.subject.keywordPlus | EFFICIENT SYNTHESIS | - |
dc.subject.keywordPlus | PHENYLACETIC ACIDS | - |
dc.subject.keywordPlus | BOND ACTIVATION | - |
dc.subject.keywordPlus | DERIVATIVES | - |
dc.subject.keywordPlus | CYCLIZATION | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
(02841) 서울특별시 성북구 안암로 14502-3290-1114
COPYRIGHT © 2021 Korea University. All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.