Publication: Destannylative acylation of 1-[(2-methoxyethoxy)methoxy]-2- (phenylsulfonyl)-2-(tributylstannyl)cyclopropane: A novel route to 3- acylfurans
dc.contributor.author | Manat Pohmakotr | en_US |
dc.contributor.author | Auntika Takampon | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-07-04T07:21:54Z | |
dc.date.available | 2018-07-04T07:21:54Z | |
dc.date.issued | 1996-06-24 | en_US |
dc.description.abstract | Destannylative acylation of 1-[(2-methoxyethoxy)methoxy]-2- (phenylsulfonyl)-2-(tributylstannyl)cyclopropane (1) provided dihydrofurans 5 in good yields, which upon treatment with BF3.OEt2in CH2Cl2led to the formation of 3-acylfurans 6 in moderate yields. The reaction was proposed to proceed via the intramolecular Prins-type reaction of the oxonium intermediate 7. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.37, No.26 (1996), 4585-4588 | en_US |
dc.identifier.doi | 10.1016/0040-4039(96)00852-0 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-0030600152 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/17541 | |
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=0030600152&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 | Destannylative acylation of 1-[(2-methoxyethoxy)methoxy]-2- (phenylsulfonyl)-2-(tributylstannyl)cyclopropane: A novel route to 3- acylfurans | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0030600152&origin=inward | en_US |