Publication: A facile synthesis of telisatin A via microwave-promoted annulation and reformatsky reaction
| dc.contributor.author | Nopporn Thasana | en_US |
| dc.contributor.author | Ben Bjerke-Kroll | en_US |
| dc.contributor.author | Somsak Ruchirawat | en_US |
| dc.contributor.other | Chulabhorn Graduate Institute | 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 | 2018-07-12T02:23:19Z | |
| dc.date.available | 2018-07-12T02:23:19Z | |
| dc.date.issued | 2008-03-03 | en_US |
| dc.description.abstract | A facile one-pot synthesis of 2,3-dioxopyrrolo[2,1-a]isoquinolines is reported involving the ring formation of aryl pyruvate derivatives with 3,4-dihydroisoquinolines under basic conditions and utilizing the Reformatsky reaction. Using microwave irradiation, the required compounds were obtained in moderate to good yields. © Georg Thieme Verlag Stuttgart. | en_US |
| dc.identifier.citation | Synlett. No.4 (2008), 505-508 | en_US |
| dc.identifier.doi | 10.1055/s-2008-1042764 | en_US |
| dc.identifier.issn | 09365214 | en_US |
| dc.identifier.other | 2-s2.0-40949157622 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/19088 | |
| 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=40949157622&origin=inward | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | A facile synthesis of telisatin A via microwave-promoted annulation and reformatsky reaction | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40949157622&origin=inward | en_US |