Reaction of N,N '-disubstituted hydrazinecarbothioamides with 2-bromo-2-substituted acetophenones

Show simple item record Aly, Ashraf A. Hassan, Alaa A. AbdAl-Latif, El-Shimaa S. M. Ibrahim, Mahmoud A. A. Bräse, Stefan Nieger, Martin 2018-08-10T06:42:01Z 2018-08-10T06:42:01Z 2018
dc.identifier.citation Aly , A A , Hassan , A A , AbdAl-Latif , E-S S M , Ibrahim , M A A , Bräse , S & Nieger , M 2018 , ' Reaction of N,N '-disubstituted hydrazinecarbothioamides with 2-bromo-2-substituted acetophenones ' , ARKIVOC , pp. 102-111 .
dc.identifier.other PURE: 115028872
dc.identifier.other PURE UUID: e5bc4cc9-04a4-4369-9595-8cdcd29eb3ca
dc.identifier.other WOS: 000438799100008
dc.identifier.other Scopus: 85041113478
dc.identifier.other ORCID: /0000-0003-1677-0109/work/47426048
dc.description.abstract Reaction of hydrazinecarbothioamides with 2-bromoacetophenones furnished the formation of thiazole-, bis-thiazole-, pyrazole- and 1,3,4-thiadiazole- derivatives in good yields. The mechanism was discussed. The structures of products were proved by MS, IR, NMR, elemental analyses and X-ray structure analyses. [GRAPHICS] . en
dc.format.extent 10
dc.language.iso eng
dc.relation.ispartof ARKIVOC
dc.rights unspecified
dc.rights.uri info:eu-repo/semantics/openAccess
dc.subject Hydrazinecarbothioamides
dc.subject 2-bromoacetophenones
dc.subject thiazoles
dc.subject bis-thiazole
dc.subject pyrazole
dc.subject DERIVATIVES
dc.subject INHIBITORS
dc.subject MOIETIES
dc.subject SERIES
dc.subject AGENTS
dc.subject ETHYL
dc.subject 116 Chemical sciences
dc.title Reaction of N,N '-disubstituted hydrazinecarbothioamides with 2-bromo-2-substituted acetophenones en
dc.type Article
dc.contributor.organization Department of Chemistry
dc.description.reviewstatus Peer reviewed
dc.relation.issn 1551-7004
dc.rights.accesslevel openAccess
dc.type.version publishedVersion

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