Publication:
A facile two-step synthesis of thiophene end-capped aromatic systems

dc.contributor.authorBunyarat Rungtaweevoraniten_US
dc.contributor.authorAkkarapol Butsurien_US
dc.contributor.authorKrittaphat Wongmaen_US
dc.contributor.authorKaroon Sadornen_US
dc.contributor.authorKitjanit Neranonen_US
dc.contributor.authorChakkrapan Nerungsien_US
dc.contributor.authorTienthong Thongpanchangen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.date.accessioned2018-06-11T04:37:51Z
dc.date.available2018-06-11T04:37:51Z
dc.date.issued2012-04-04en_US
dc.description.abstractThiophene end-capped aromatic analogues, that is, naphthothiophenes, naphthodithiophenes, pyrenothiophene, and benzotrithiophene, can be prepared from commercially available hydroxyarenes in two steps, including (1) a consecutive acid-mediated nucleophilic aromatic substitution of hydroxyarenes with 2-mercaptoethanol, followed by cyclization to form an arene-fused dihydrothiophene, and (2) oxidation of the dihydrothiophene unit to thiophene. © 2012 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.53, No.14 (2012), 1816-1818en_US
dc.identifier.doi10.1016/j.tetlet.2012.01.122en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-84857789975en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/13762
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84857789975&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA facile two-step synthesis of thiophene end-capped aromatic systemsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84857789975&origin=inwarden_US

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