Publication: Two protocols for the conversion of biphenol to binaphthol: Synthesis of diospyrol
| dc.contributor.author | Nopporn Thasana | en_US |
| dc.contributor.author | Somchai Pisutjaroenpong | 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 | 2018-08-20T06:56:00Z | |
| dc.date.available | 2018-08-20T06:56:00Z | |
| dc.date.issued | 2006-05-03 | en_US |
| dc.description.abstract | The application of directed orthometallation (DoM), Fries rearrangement and transmetallation followed by allylation and cyclization is reported for the conversion of biphenol to binaphthol as a means for the synthesis of diospyrol. Furthermore, the same transformation can be accomplished by the reaction of the dienolate anion of an α,β-unsaturated amide with an aryne intermediate. © Georg Thieme Verlag Stuttgart. | en_US |
| dc.identifier.citation | Synlett. No.7 (2006), 1080-1084 | en_US |
| dc.identifier.doi | 10.1055/s-2006-939075 | en_US |
| dc.identifier.issn | 09365214 | en_US |
| dc.identifier.other | 2-s2.0-33646548606 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/23164 | |
| 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=33646548606&origin=inward | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Two protocols for the conversion of biphenol to binaphthol: Synthesis of diospyrol | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33646548606&origin=inward | en_US |