Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions

© 2018 Georg Thieme Verlag Stuttgart New York - Synthesis. A highly efficient iodine-catalyzed oxidative cross-dehydrogenative coupling reaction of quinoxalinones and indoles has been developed. Without the requirement of peroxide and acid, this reaction utilizes a catalytic amount of molecular iodi...

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Main Authors: Medena Noikham, Tanakorn Kittikool, Sirilata Yotphan
Other Authors: Mahidol University
Format: Article
Published: 2019
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/45424
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spelling th-mahidol.454242019-08-23T17:49:59Z Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions Medena Noikham Tanakorn Kittikool Sirilata Yotphan Mahidol University Chemical Engineering Chemistry © 2018 Georg Thieme Verlag Stuttgart New York - Synthesis. A highly efficient iodine-catalyzed oxidative cross-dehydrogenative coupling reaction of quinoxalinones and indoles has been developed. Without the requirement of peroxide and acid, this reaction utilizes a catalytic amount of molecular iodine to facilitate the C-C bond formation under ambient air. This simple and easy-to-handle protocol represents an interesting synthetic alternative with a good scope and functional group compatibility. 2019-08-23T10:45:15Z 2019-08-23T10:45:15Z 2018-06-15 Article Synthesis (Germany). Vol.50, No.12 (2018), 2337-2346 10.1055/s-0037-1609445 1437210X 00397881 2-s2.0-85045136757 https://repository.li.mahidol.ac.th/handle/123456789/45424 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85045136757&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 Chemical Engineering
Chemistry
spellingShingle Chemical Engineering
Chemistry
Medena Noikham
Tanakorn Kittikool
Sirilata Yotphan
Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions
description © 2018 Georg Thieme Verlag Stuttgart New York - Synthesis. A highly efficient iodine-catalyzed oxidative cross-dehydrogenative coupling reaction of quinoxalinones and indoles has been developed. Without the requirement of peroxide and acid, this reaction utilizes a catalytic amount of molecular iodine to facilitate the C-C bond formation under ambient air. This simple and easy-to-handle protocol represents an interesting synthetic alternative with a good scope and functional group compatibility.
author2 Mahidol University
author_facet Mahidol University
Medena Noikham
Tanakorn Kittikool
Sirilata Yotphan
format Article
author Medena Noikham
Tanakorn Kittikool
Sirilata Yotphan
author_sort Medena Noikham
title Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions
title_short Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions
title_full Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions
title_fullStr Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions
title_full_unstemmed Iodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient Conditions
title_sort iodine-catalyzed oxidative cross-dehydrogenative coupling of quinoxalinones and indoles: synthesis of 3-(indol-2-yl)quinoxalin-2-one under mild and ambient conditions
publishDate 2019
url https://repository.li.mahidol.ac.th/handle/123456789/45424
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