Publication:
α-(Phenylthio)cyclopropylation of carbonyl compounds: Preparation of α-cyclopropyl ketones

Simple item page
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorJirakorn Thisayuktaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-04T07:40:11Z
dc.date.available2018-07-04T07:40:11Z
dc.date.issued1997-09-22en_US
dc.description.abstractα-Chloro-α-(phenylthio)cyclopropane and α-acetoxy-α-(phenylthio)cyclopropane were found to react with the silyl enol ethers of some ketones in the presence of Lewis acid in dichloromethane to provide α-(phenylthio)cyclopropyl ketones, which were subjected to reduction with Ra-Ni to give the corresponding α-cyclopropyl ketones.en_US
dc.identifier.citationTetrahedron Letters. Vol.38, No.38 (1997), 6759-6762en_US
dc.identifier.doi10.1016/S0040-4039(97)01546-3en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0030821569en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/17880
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0030821569&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleα-(Phenylthio)cyclopropylation of carbonyl compounds: Preparation of α-cyclopropyl ketonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0030821569&origin=inwarden_US

Files

Collections

Scopus 1991-2000