Publication: Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones
dc.contributor.author | Manat Pohmakotr | en_US |
dc.contributor.author | Supatara Popuang | en_US |
dc.contributor.author | Sirirat Chancharunee | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-06-14T09:12:53Z | |
dc.date.available | 2018-06-14T09:12:53Z | |
dc.date.issued | 1989-01-01 | en_US |
dc.description.abstract | A convenient synthesis of 4-hydroxy spiro[4.n]alk-2-ene-1-ones and spiro [4.n] alk-2-ene-1,4-diones, which involves the intramolecular acylation of α-sulfinyl carbanions followed by pyrolysis and/or oxidation, is described. © 1989. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.30, No.13 (1989), 1715-1718 | en_US |
dc.identifier.doi | 10.1016/S0040-4039(00)99563-7 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-0000598807 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/15721 | |
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=0000598807&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 | Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0000598807&origin=inward | en_US |