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Article: Regioselective Debromination of 2,3,5-Tribromothiophene: A Facile Synthesis of Isomerically Pure 2,3- and 2,4-Dibromothiophene

TitleRegioselective Debromination of 2,3,5-Tribromothiophene: A Facile Synthesis of Isomerically Pure 2,3- and 2,4-Dibromothiophene
Authors
Issue Date1996
Citation
Journal of Chemical Research - Part S, 1996, n. 3, p. 150-151 How to Cite?
AbstractThe regioselective preparative debromination of 2,3,5-tribromothiophene to isomerically pure 2,3- and 2,4-dibromothiophene was effected by the use of sodium borohydride in the presence and absence of transition metal catalyst using predetermined optimum conditions from GC trials.
Persistent Identifierhttp://hdl.handle.net/10722/219498
ISSN
2009 Impact Factor: 0.61
2006 SCImago Journal Rankings: 0.166

 

DC FieldValueLanguage
dc.contributor.authorXie, Yang-
dc.contributor.authorNg, Siu Choon-
dc.contributor.authorHor, T. S Andy-
dc.contributor.authorChan, Hardy S O-
dc.date.accessioned2015-09-23T02:57:14Z-
dc.date.available2015-09-23T02:57:14Z-
dc.date.issued1996-
dc.identifier.citationJournal of Chemical Research - Part S, 1996, n. 3, p. 150-151-
dc.identifier.issn0308-2342-
dc.identifier.urihttp://hdl.handle.net/10722/219498-
dc.description.abstractThe regioselective preparative debromination of 2,3,5-tribromothiophene to isomerically pure 2,3- and 2,4-dibromothiophene was effected by the use of sodium borohydride in the presence and absence of transition metal catalyst using predetermined optimum conditions from GC trials.-
dc.languageeng-
dc.relation.ispartofJournal of Chemical Research - Part S-
dc.titleRegioselective Debromination of 2,3,5-Tribromothiophene: A Facile Synthesis of Isomerically Pure 2,3- and 2,4-Dibromothiophene-
dc.typeArticle-
dc.description.natureLink_to_subscribed_fulltext-
dc.identifier.scopuseid_2-s2.0-2742586036-
dc.identifier.issue3-
dc.identifier.spage150-
dc.identifier.epage151-

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