Publication: Application of the hypervalent iodine reagent to the synthesis of some pentasubstituted aporphine alkaloids
| dc.contributor.author | Ratchanok Pingaew | en_US |
| dc.contributor.author | Somsak Ruchirawat | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.contributor.other | Chulabhorn Research Institute | en_US |
| dc.contributor.other | The Institute of Science and Technology for Research and Development, Mahidol University | en_US |
| dc.date.accessioned | 2018-08-24T01:45:55Z | |
| dc.date.available | 2018-08-24T01:45:55Z | |
| dc.date.issued | 2007-09-17 | en_US |
| dc.description.abstract | The oxidative biaryl coupling of various N-substituted 1- benzyltetrahydroisoquinolines to the corresponding aporphines by the hypervalent iodine reagent was studied. The study sheds light on the unifying mechanism of the reaction illustrating the requirement of the p-p coupling via the six-membered transition state as the initial step. The finding was applied to the synthesis of some pentasubstituted aporphine alkaloids. © Georg Thieme Verlag Stuttgart. | en_US |
| dc.identifier.citation | Synlett. No.15 (2007), 2363-2366 | en_US |
| dc.identifier.doi | 10.1055/s-2007-985596 | en_US |
| dc.identifier.issn | 09365214 | en_US |
| dc.identifier.other | 2-s2.0-34948839846 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/24337 | |
| 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=34948839846&origin=inward | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Application of the hypervalent iodine reagent to the synthesis of some pentasubstituted aporphine alkaloids | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34948839846&origin=inward | en_US |