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DC Field | Value | Language |
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dc.contributor.author | Sutthichat Kerdphon | en_US |
dc.contributor.author | Patthadon Sanghong | en_US |
dc.contributor.author | Jaruwan Chatwichien | en_US |
dc.contributor.author | Vachira Choommongkol | en_US |
dc.contributor.author | Puracheth Rithchumpon | en_US |
dc.contributor.author | Thishana Singh | en_US |
dc.contributor.author | Puttinan Meepowpan | en_US |
dc.date.accessioned | 2020-10-14T08:29:04Z | - |
dc.date.available | 2020-10-14T08:29:04Z | - |
dc.date.issued | 2020-05-14 | en_US |
dc.identifier.issn | 10990690 | en_US |
dc.identifier.issn | 1434193X | en_US |
dc.identifier.other | 2-s2.0-85084550137 | en_US |
dc.identifier.other | 10.1002/ejoc.202000257 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85084550137&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/70395 | - |
dc.description.abstract | © 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim The focus of this study was the development of a new synthetic method for quinazolinones based on the principles of Green Chemistry. Quinazolinones were synthesized from 2-aminobenzamide using methanol as both the C1 source and a green solvent in the presence of base Cs2CO3. Additionally, a commercially available, economical copper complex was used as a catalyst in the reaction. The desired products were achieved in moderate to high yield with up to 99 % isolated yield. | en_US |
dc.subject | Chemistry | en_US |
dc.title | Commercial Copper-Catalyzed Aerobic Oxidative Synthesis of Quinazolinones from 2-Aminobenzamide and Methanol | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | European Journal of Organic Chemistry | en_US |
article.volume | 2020 | en_US |
article.stream.affiliations | Naresuan University | en_US |
article.stream.affiliations | Maejo University | en_US |
article.stream.affiliations | University of KwaZulu-Natal | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Chulabhorn Royal Academy | en_US |
Appears in Collections: | CMUL: Journal Articles |
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