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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/76878
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dc.titleRegioselective Debromination of 2,3,5-Tribromothiophene: A Facile Synthesis of Isomerically Pure 2,3- and 2,4-Dibromothiophene
dc.contributor.authorXie, Y.
dc.contributor.authorNg, S.-C.
dc.contributor.authorHor, T.S.A.
dc.contributor.authorChan, H.S.O.
dc.date.accessioned2014-06-23T05:48:13Z
dc.date.available2014-06-23T05:48:13Z
dc.date.issued1996-03
dc.identifier.citationXie, Y.,Ng, S.-C.,Hor, T.S.A.,Chan, H.S.O. (1996-03). Regioselective Debromination of 2,3,5-Tribromothiophene: A Facile Synthesis of Isomerically Pure 2,3- and 2,4-Dibromothiophene. Journal of Chemical Research - Part S (3) : 150-151. ScholarBank@NUS Repository.
dc.identifier.issn03082342
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76878
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.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleJournal of Chemical Research - Part S
dc.description.issue3
dc.description.page150-151
dc.description.codenJRPSD
dc.identifier.isiutNOT_IN_WOS
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