Publication: A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions
dc.contributor.author | Manat Pohmakotr | en_US |
dc.contributor.author | Tanasri Bunlaksananusorn | en_US |
dc.contributor.author | Patoomratana Tuchinda | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-09-07T09:08:44Z | |
dc.date.available | 2018-09-07T09:08:44Z | |
dc.date.issued | 2000-01-15 | en_US |
dc.description.abstract | A convenient and general synthetic method for spiro[4.n]alk-2-ene-1,6- diones and spiro[5.n]alk-2-ene-1,7-diones, which involves the intramolecular acylation of an α-sulfinyl carbanion, is described. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.41, No.3 (2000), 377-380 | en_US |
dc.identifier.doi | 10.1016/S0040-4039(99)01897-3 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-0034650831 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/25880 | |
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=0034650831&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 | A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation 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=0034650831&origin=inward | en_US |