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SYNTHESIS OF NEW THIO-SUBSTITUTED BUTADIENES USING 1,3-DI-H-TETRACHLOROBUTADIENE AND 2H-PENTACHLOROBUTADIENE

dc.contributor.authorIBIS, C
dc.contributor.authorSAYIL, C
dc.date.accessioned2021-03-03T19:40:33Z
dc.date.available2021-03-03T19:40:33Z
dc.identifier.citationIBIS C., SAYIL C., "SYNTHESIS OF NEW THIO-SUBSTITUTED BUTADIENES USING 1,3-DI-H-TETRACHLOROBUTADIENE AND 2H-PENTACHLOROBUTADIENE", PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, cilt.86, ss.55-59, 1994
dc.identifier.issn0308-664X
dc.identifier.othervv_1032021
dc.identifier.otherav_55e4c66a-39c9-4673-8934-53edf0ffc88d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/60658
dc.identifier.urihttps://doi.org/10.1080/10426509408018387
dc.description.abstractCompounds 3a, 4a, 6a, 5b, 6b, 3c, 3d, 3f, and 5e, have been obtained from 1,3-di-H-tetrachlorobutadiene 1 and thiolates in DMSO at room temperature. With the same conditions 2H-pentachlorobutadiene 7 and thiolates give compounds 8a, 9a, 8c, 9c, 84, 94 and 9f. Hexachlorobutene 10 with benzylthiolate forms compound 12 in DMSO. The reaction of compounds 3e and 3d, with 3-chloroperbenzoic acid forms sulfoxide compounds 13c and 13d in chloroform, respectively. The structure of the reaction products was established by spectroscopic techniques.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKİMYA, İNORGANİK VE NÜKLEER
dc.subjectBiyokimya
dc.subjectBiyoinorganik Kimya
dc.subjectİnorganik Kimya
dc.subjectTemel Bilimler
dc.subjectKİMYA, ORGANİK
dc.titleSYNTHESIS OF NEW THIO-SUBSTITUTED BUTADIENES USING 1,3-DI-H-TETRACHLOROBUTADIENE AND 2H-PENTACHLOROBUTADIENE
dc.typeMakale
dc.relation.journalPHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
dc.contributor.department, ,
dc.identifier.volume86
dc.identifier.startpage55
dc.identifier.endpage59
dc.contributor.firstauthorID114970


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