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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Wong Phakhodee | en_US |
| dc.contributor.author | Sirilak Wangngae | en_US |
| dc.contributor.author | Mookda Pattarawarapan | en_US |
| dc.date.accessioned | 2018-09-05T03:32:51Z | - |
| dc.date.available | 2018-09-05T03:32:51Z | - |
| dc.date.issued | 2017-08-04 | en_US |
| dc.identifier.issn | 15206904 | en_US |
| dc.identifier.issn | 00223263 | en_US |
| dc.identifier.other | 2-s2.0-85027057783 | en_US |
| dc.identifier.other | 10.1021/acs.joc.7b01322 | en_US |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027057783&origin=inward | en_US |
| dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/56972 | - |
| dc.description.abstract | © 2017 American Chemical Society. Readily available N-substituted amides or their requisite carboxylic acids or acid chlorides have been used to construct 2,3-disubstituted-3H-quinazolin-4-ones in a one-pot procedure. Key transformation in this convergent approach involves Ph3P-I2-mediated formation of amidine upon condensation of an amide or the intermediate amide with methyl anthranilate. Cyclization of the amidine-tethered anthranilate then affords 2,3-disubstituted-3H-quinazolin-4-ones in good to excellent yields under mild conditions. | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Approach to the Synthesis of 2,3-Disubstituted-3H-quinazolin-4-ones Mediated by Ph<inf>3</inf>P-I<inf>2</inf> | en_US |
| dc.type | Journal | en_US |
| article.title.sourcetitle | Journal of Organic Chemistry | en_US |
| article.volume | 82 | en_US |
| article.stream.affiliations | Chiang Mai University | en_US |
| Appears in Collections: | CMUL: Journal Articles | |
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