Publication: Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
| dc.contributor.author | Wong Phakhodee | en_US |
| dc.contributor.author | Poolsak Sahakitpichan | en_US |
| dc.contributor.author | Songpon Deechongkit | en_US |
| dc.contributor.author | Somsak Ruchirawat | en_US |
| dc.contributor.other | Chulabhorn Research Institute | en_US |
| dc.contributor.other | Chulabhorn Graduate Institute | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.contributor.other | The Institute of Science and Technology for Research and Development, Mahidol University | en_US |
| dc.date.accessioned | 2018-07-12T02:22:33Z | |
| dc.date.available | 2018-07-12T02:22:33Z | |
| dc.date.issued | 2008-08-01 | en_US |
| dc.description.abstract | On treatment with acids, the open-chained amide acetals (1) gave the 7,7 membered ring fused benzazepinones (4) via the bis-cyclisation. © 2008 The Japan Institute of Heterocyclic Chemistry. | en_US |
| dc.identifier.citation | Heterocycles. Vol.75, No.8 (2008), 1963-1970 | en_US |
| dc.identifier.doi | 10.3987/COM-08-11366 | en_US |
| dc.identifier.issn | 03855414 | en_US |
| dc.identifier.other | 2-s2.0-54249159680 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/19074 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=54249159680&origin=inward | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
| dc.title | Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=54249159680&origin=inward | en_US |