Publication: A general synthetic route to 1-azabicyclo[m.n.0]alkenes via cyclisation based on α-sulfinyl carbanions
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.author | Pornthep Numechai | en_US |
| dc.contributor.author | Saisuree Prateeptongkum | en_US |
| dc.contributor.author | Patoomratana Tuchinda | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-07-24T03:18:46Z | |
| dc.date.available | 2018-07-24T03:18:46Z | |
| dc.date.issued | 2003-10-21 | en_US |
| dc.description.abstract | A general synthetic route to 1-azabicyclo[m.n.0]alkenes via cyclisation based on α-sulfinyl carbanions was presented. The intramolecular nucleophillic addition of α-sulfinyl carbanions afforded 1-azabicyclo[m.n.0]alkenes in good yields. It is reported that the developed strategy should provide a general solution for the synthesis of various classes of 1-azabicyclic alkaloids. | en_US |
| dc.identifier.citation | Organic and Biomolecular Chemistry. Vol.1, No.20 (2003), 3495-3497 | en_US |
| dc.identifier.doi | 10.1039/b308383g | en_US |
| dc.identifier.issn | 14770520 | en_US |
| dc.identifier.other | 2-s2.0-0142227212 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/20684 | |
| 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=0142227212&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | A general synthetic route to 1-azabicyclo[m.n.0]alkenes via cyclisation based on 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=0142227212&origin=inward | en_US |