Publication: Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
| dc.contributor.author | Poolsak Sahakitpichan | en_US |
| dc.contributor.author | Nopporn Thasana | en_US |
| dc.contributor.author | Somsak Ruchirawat | 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 | 2018-06-21T08:11:16Z | |
| dc.date.available | 2018-06-21T08:11:16Z | |
| dc.date.issued | 2005-11-03 | en_US |
| dc.description.abstract | Tetramethoxydiospyrol was synthesized via Suzuki-Miyaura cross-coupling of the two key intermediates, halonaphthalene and naphthaleneboronic acid derivatives, which were derived from the same naphthol. Moreover, the product could be conveniently obtained by a one-pot modified in situ Suzuki coupling. The naphthol was synthesized via the cyclization of ortho-allylbenzamide intermediate. © Georg Thieme Verlag Stuttgart. | en_US |
| dc.identifier.citation | Synthesis. No.17 (2005), 2934-2938 | en_US |
| dc.identifier.doi | 10.1055/s-2005-872176 | en_US |
| dc.identifier.issn | 00397881 | en_US |
| dc.identifier.other | 2-s2.0-27944482117 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/16411 | |
| 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=27944482117&origin=inward | en_US |
| dc.subject | Chemical Engineering | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27944482117&origin=inward | en_US |