Publication: Asymmetric synthesis of ent-fragransin C<inf>1</inf>
| dc.contributor.author | Santikorn Chaimanee | en_US |
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.author | Chutima Kuhakarn | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.author | Darunee Soorukram | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-12-21T06:57:11Z | |
| dc.date.accessioned | 2019-03-14T08:03:04Z | |
| dc.date.available | 2018-12-21T06:57:11Z | |
| dc.date.available | 2019-03-14T08:03:04Z | |
| dc.date.issued | 2017-01-01 | en_US |
| dc.description.abstract | © 2017 The Royal Society of Chemistry. The first asymmetric synthesis of ent-fragransin C1was reported. The key step involves an intramolecular C-O bond formation (furan ring formation) via chemoselective generation of the benzylic carbocation leading to the 2,3-anti-3,4-syn-4,5-anti-tetrahydrofuran moiety as a single diastereomer in good yield. Our synthesis confirms that ent-fragransin C1possesses 2R,3R,4S,5S configurations. | en_US |
| dc.identifier.citation | Organic and Biomolecular Chemistry. Vol.15, No.18 (2017), 3985-3994 | en_US |
| dc.identifier.doi | 10.1039/c7ob00749c | en_US |
| dc.identifier.issn | 14770520 | en_US |
| dc.identifier.other | 2-s2.0-85021655664 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/42053 | |
| 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=85021655664&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Asymmetric synthesis of ent-fragransin C<inf>1</inf> | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85021655664&origin=inward | en_US |