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α-Bromination of linear enals and cyclic enones

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dc.contributor.authorPakorn Bovonsombaten_US
dc.contributor.authorRungkarn Rujiwarangkulen_US
dc.contributor.authorThanathip Bowornkiengkaien_US
dc.contributor.authorJuthamard Leykajarakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-24T01:39:13Z
dc.date.available2018-08-24T01:39:13Z
dc.date.issued2007-12-03en_US
dc.description.abstractFacile α-bromination of cyclic enones and linear enals involving N-bromosuccinimide and 1-2 equiv of pyridine-N-oxide is reported herein. α-Bromination of linear enals was found to proceed with double bond geometry retention. © 2007 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.48, No.49 (2007), 8607-8610en_US
dc.identifier.doi10.1016/j.tetlet.2007.10.055en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-35748952212en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/24063
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=35748952212&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleα-Bromination of linear enals and cyclic enonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=35748952212&origin=inwarden_US

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