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1,3,4-Thiadiazines: Methods of synthesis and reactivity (review)
Chemistry of Heterocyclic Compounds, 1991The synthetic methods for 1,3,4-thiadiazines and their intramolecular rearrangement reactions are reviewed.
S. V. Usol'tseva +2 more
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Synthesis and transformations of 2-amino-1,3,4-thiadiazines
Chemistry of Heterocyclic Compounds, 1991Depending on the reaction conditions, 2-amino-1,3,4-thiadiazine and 2-hydrazinothiazole derivatives were obtained by cyclization of thiosemicarbazide with ethyl bromopyruvate in concentrated hydrochloric acid. The rearrangements of 5-carbonyl-substituted 2-amino-1,3,4-thiadiazines to thiazole derivatives in an acidic medium were studied.
S. V. Usol'tseva +4 more
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ChemInform Abstract: 1,3,4‐Thiadiazines: Synthesis and Reactivity
ChemInform, 1992AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. V. USOL'TSEVA +2 more
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Novel Synthesis of 1,3,4‐Thiadiazine Derivatives and Their Cycloaddition Reactions.
ChemInform, 2006AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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ChemInform, 2008
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Radineh Motamedi +3 more
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Radineh Motamedi +3 more
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Synthesis and Reactivity of 3,4-Dimethyl-4H-1,3,4-thiadiazines
Synlett, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Wolf‐Diethard Pfeiffer +3 more
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Diastereoselective synthesis of 3,6-dihydro-2H-1,3,4-thiadiazines
Tetrahedron: Asymmetry, 1998Abstract Thionation of the benzil hydrazones 3 with Lawesson's reagent afforded the 3,6-dihydro-2 H -1,3,4-thiadiazines 4 by an intramolecular cyclisation. This reaction was shown to be diastereospecific and allowed the formation of the exo compounds 4b – e .
Jean-Damien Charrier +2 more
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ChemInform Abstract: Synthesis of 1,3,4‐Thiadiazines and 1,3,4‐Oxadiazines
ChemInform, 1999AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Ho Sik Kim, Yoshihisa Kurasawa
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ChemInform Abstract: THE CHEMISTRY OF A 1,3,4‐THIADIAZIN‐6‐ONE
Chemischer Informationsdienst, 1982AbstractDas Thiosemicarbazon (I) cyclisiert in Gegenwart von Dicyclohexylcarbodiimid (DCC) zum Dimethylamino‐phenyl‐thiadiazinon (II), das bei der Blitzvakuumpyrolyse unter Abspaltung von (IV) und (V) zum Thiadiazol (III) führt.
A. E. BAYDAR, G. V. BOYD, P. F. LINDLEY
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Pharmaceutical Chemistry Journal, 2020
A group of novel 2-propylmorpholino-5-aryl- and 5-thienyl-6H-1,3,4-thiadiazine dihydrobromides was synthesized by cyclocondensation of 4-[3-(4-morpholino)propyl]-3-thiosemicarbazide with α –haloacetoarenones or α-haloacetylthiophenones. Two compounds of this group were found to produce effective inhibition of non-enzymatic protein glycation in an in ...
T. A. Tseitler +4 more
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A group of novel 2-propylmorpholino-5-aryl- and 5-thienyl-6H-1,3,4-thiadiazine dihydrobromides was synthesized by cyclocondensation of 4-[3-(4-morpholino)propyl]-3-thiosemicarbazide with α –haloacetoarenones or α-haloacetylthiophenones. Two compounds of this group were found to produce effective inhibition of non-enzymatic protein glycation in an in ...
T. A. Tseitler +4 more
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