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dc.contributor.authorDeniz, N. Gulsah
dc.contributor.authorIbis, Cemil
dc.date.accessioned2021-03-06T13:01:56Z
dc.date.available2021-03-06T13:01:56Z
dc.date.issued2007
dc.identifier.citationIbis C., Deniz N. G. , "The novel N, S-substituted nitro dienes from the reactions of some mono (alkylthio)-substituted 2-nitrodienes with piperazine and thiomorpholine and a structural study", INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, cilt.46, ss.674-680, 2007
dc.identifier.issn0376-4699
dc.identifier.othervv_1032021
dc.identifier.otherav_f6c0556e-893b-4ea1-8022-256fbe334cc4
dc.identifier.urihttp://hdl.handle.net/20.500.12627/161647
dc.description.abstractThiosubstituted nitrodien compounds 1a-f are obtained from 2-nitropentachlorobutadiene and some alifatic thiols. Compounds 1a-f have reacted with thiomorpholine 2 and yielded 3a-f in CH2Cl2. The compounds 5a-f have been obtained by the reactions of 1a-f with N-(diphenylmethyl)piperazine 4 in CH2Cl2. 2-Nitro-3,4,4-trichloro-1-(ethylthio)-1-[4-(1-diphenylmethyl)-piperazin-1-yl]-1,3-butadiene 5a is synthesized and its crystal structure is determined. The compound 5a crystallizes in the orthorhombic crystal system (space group P2(1)2(1)2(1)) with the unit cell parameters a = 9.4240(2) angstrom, b = 14.4007(2) angstrom, c = 18.1891(2) angstrom, alpha, beta, gamma = 90 degrees, V = 2468.48(7) angstrom(3), Z = 4. The structure has been solved by direct methods (SIR92) and refined to the residual index R-1 = 0.078.
dc.language.isoeng
dc.subjectBiyokimya
dc.subjectBiyoinorganik Kimya
dc.subjectTemel Bilimler
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKİMYA, ORGANİK
dc.titleThe novel N, S-substituted nitro dienes from the reactions of some mono (alkylthio)-substituted 2-nitrodienes with piperazine and thiomorpholine and a structural study
dc.typeMakale
dc.relation.journalINDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY
dc.contributor.department, ,
dc.identifier.volume46
dc.identifier.issue4
dc.identifier.startpage674
dc.identifier.endpage680
dc.contributor.firstauthorID182264


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