Publication: Synthesis of (+)-lentiginosine and its pyrrolizidine analogue based on intramolecular cyclization of α-sulfinyl carbanions
| dc.contributor.author | Sakkarin Du-A-Man | en_US |
| dc.contributor.author | Darunee Soorukram | en_US |
| dc.contributor.author | Chutima Kuhakarn | en_US |
| dc.contributor.author | Patoomratana Tuchinda | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-11-09T02:06:12Z | |
| dc.date.available | 2018-11-09T02:06:12Z | |
| dc.date.issued | 2014-03-01 | en_US |
| dc.description.abstract | A synthesis of (+)-lentiginosine and its pyrrolizidine analogue was accomplished in six steps, starting from L-(+)-tartaric acid. The key step of these syntheses involves the intramolecular cyclization of α-sulfinyl carbanions for the construction of the indolizidine or pyrrolizidine ring. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_US |
| dc.identifier.citation | European Journal of Organic Chemistry. Vol.2014, No.8 (2014), 1708-1715 | en_US |
| dc.identifier.doi | 10.1002/ejoc.201301671 | en_US |
| dc.identifier.issn | 10990690 | en_US |
| dc.identifier.issn | 1434193X | en_US |
| dc.identifier.other | 2-s2.0-84897628501 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/33628 | |
| 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=84897628501&origin=inward | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Synthesis of (+)-lentiginosine and its pyrrolizidine analogue based on intramolecular cyclization of α-sulfinyl carbanions | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84897628501&origin=inward | en_US |