Journal ArticleDOI
Novel 1,2,3-thiadiazolyl sulfines from the reaction of N-substituted hydrazones with thionyl chloride
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This article is published in Journal of Organic Chemistry.The article was published on 1984-12-01. It has received 20 citations till now. The article focuses on the topics: Thionyl chloride & Hydrazone.read more
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[3+2]-cycloadditions of 1-Aza-2-azoniaallene cations to multiple bonds
TL;DR: In this article, 1-chloroalkylazo compounds were transformed into 1-aza-2-azoniaallene salts, and the cycloadducts undergo consecutive reactions, e.g. [1, 2]-shifts of alkyl groups.
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Synthesis and antibacterial activity of some 5-(4-biphenylyl)-7-aryl[3,4-d] [1,2,3]-benzothiadiazoles.
TL;DR: A series of 5-(4-biphenylyl)-7-aryl[3,4-d] [1,2,3]-benzothiadiazoles were synthesized, characterized by IR, NMR and elemental analysis and evaluated for in vitro antibacterial activity against some Gram-positive and Gram-negative bacteria.
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Application of the hurd-mori-reaction for the synthesis of tricyclic annelated 1,2,3-thiadiazoles
TL;DR: In this paper, a mechanism for the aromatization step with thionyl chloride is proposed, based on the results of the Hurd-Mori reaction in the key step, which yields the fully aromatic products, instead of the expected annelated 4,5-dihydro[1,2,3]thiadiazoles.
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Synthesis and biological evaluation of 5,7-diaryl-4,4-dimethyl-4,5,6,7-tetrahydropyridino[3,4-d]-1,2,3-thiadiazoles
TL;DR: In general, all the synthesized compounds exert a wide range of modest in vitro antifungal activity against Rhizopus and Microsporum gypsuem than the standard drug, fluconazole.
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Synthetic uses of thionyl chloride
TL;DR: In this paper, an important example of such a reagent is thionyl chloride, an important reagent for synthetic organic chemistry which is readily generated and used for further exploitation.