Publication: Asymmetric synthesis of pentenomycin I, epipentenomycin I, and their analogs
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.author | Supakeat Kambutong | en_US |
| dc.contributor.author | Patoomratana Tuchinda | en_US |
| dc.contributor.author | Chutima Kuhakarn | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-07-12T02:18:16Z | |
| dc.date.available | 2018-07-12T02:18:16Z | |
| dc.date.issued | 2008-06-30 | en_US |
| dc.description.abstract | The synthetic utility of the intramolecular acylation of α-sulfinyl carbanions as an efficient and general synthetic approach for the preparation of (-)-pentenomycin I (1) and (-)-epipentenomycin I (5) and their enantiomers (ent-1 and ent-5), starting from chiral (2S,5S,6S)-ester 6 and ent-6, respectively, has been demonstrated. Easy accesses to pentenomycin analogs have also been demonstrated through the Pummerer, Suzuki-Miyaura, and Sonogashira reactions. © 2008 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.citation | Tetrahedron. Vol.64, No.27 (2008), 6315-6323 | en_US |
| dc.identifier.doi | 10.1016/j.tet.2008.04.089 | en_US |
| dc.identifier.issn | 00404020 | en_US |
| dc.identifier.other | 2-s2.0-44349090861 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/18904 | |
| 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=44349090861&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
| dc.title | Asymmetric synthesis of pentenomycin I, epipentenomycin I, and their analogs | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=44349090861&origin=inward | en_US |