Oxidations of 4 H ‐1,2,6‐Thiadiazines
Abstract The oxidation of various non‐S‐oxidized 4 H ‐1,2,6‐thiadiazines with N 2 O 4 , meta ‐chloroperbenzoic acid ( m
Andreas S. Kalogirou +2 more
wiley +3 more sources
A Qualitative Comparison of the Reactivities of 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine and 4,5-Dichloro-1,2,3-dithiazolium Chloride [PDF]
The high yielding transformations of 3,4,4,5-tetrachloro-4H-1,2,6-thiadiazine into 3,5-dichloro-4H-1,2,6-thiadiazin-4-one (up to 85%) and 2-(3,5-dichloro-4H-1,2,6-thiadiazin-4-ylidene)malononitrile (up to 83%) have been investigated and compared to the ...
Andreas S. Kalogirou +1 more
doaj +3 more sources
The Photochemical Mediated Ring Contraction of 4<i>H</i>-1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazol-3(2<i>H</i>)-one 1-Oxides. [PDF]
1,2,6-Thiadiazines treated with visible light and 3O2 under ambient conditions are converted into difficult-to-access 1,2,5-thiadiazole 1-oxides (35 examples, yields of 39–100%).
Broumidis E +12 more
europepmc +2 more sources
Novel Mono-Substituted 4H-1,2,6-Thiadiazines with Antioxidant and Anti-Lipoxygenase Activities. [PDF]
Τhe synthesis of a novel series of mono-substituted 4H-1,2,6-thiadiazine derivatives was reported, aiming at enhancing antioxidant and lipoxygenase inhibitory activities via pharmacophore combination.
Charissopoulos E +3 more
europepmc +2 more sources
Synthesis of Oligomeric 4 H ‐1,2,6‐Thiadiazines
Abstract The synthesis of oligomeric amino‐4 H ‐1,2,6‐thiadiazines, with terminal phenyl groups, containing up to four thiadiazine units is reported. The synthesis started from 3,5‐dichloro‐4 H ‐1,2,6‐thiadiazin‐4‐one and a key ...
Andreas S. Kalogirou +2 more
openaire +2 more sources
Correction to "The Photochemical Mediated Ring Contraction of 4<i>H</i>-1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazol-3(2<i>H</i>)-one 1-Oxides". [PDF]
Broumidis E +12 more
europepmc +2 more sources
Reactions of 4H-1,2,6-Thiadiazine Sulfides [PDF]
3,5-Dichloro-4H-1,2,6-thiadiazin-4-one reacts with benzo[d]thiazole-2-thiol (1 equiv) and triethylamine (1 equiv) to give 3-(benzo[d]thiazol-2-ylthio)-5-chloro-4H-1,2,6-thiadiazin-4-one in 71% yield. The reactivity of this compound with methoxide is explored and compared with that of 3-chloro-5-(phenylthio)-4H-1,2,6-thiadiazin-4-one.
Andreas S. Kalogirou +1 more
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Chemistry of 3,5‐Dichloro‐4H‐1,2,6‐thiadiazine‐4‐thione
3,5‐Dichloro‐4H‐1,2,6‐thiadiazine‐4‐thione was prepared by thionation of 3,5‐dichloro‐4H‐1,2,6‐thiadiazine‐4‐one. The chemistry of this thione was briefly investigated under thermal conditions and treatment with carbon nucleophiles, dienes and triphenylphosphine. The structures of several new products is supported by X‐ray crystallography.
Andreas S. Kalogirou +2 more
wiley +1 more source
The formation of novel α‐acyloxycarboxamides from a carboxylic acid/phenol, an aldehyde/ketone and substituted isocyanide was investigated under mechanochemical conditions in the absence of organic solvents or in the presence of a catalytic amount of H2SO4−SiO2 (solid‐assisted grinding, SAG) to create libraries of structurally complicated molecules for
Sodeeq Aderotimi Salami +3 more
wiley +1 more source
Mechanochemistry: New Tools to Navigate the Uncharted Territory of “Impossible” Reactions
Mission impossible: Mechanosynthesis is erroneously perceived as an enabling tool for only making greener well‐known solution‐based processes. Modern mechanochemistry is, above all, an effective tool to open synthetic paths not accessible by following conventional and well‐known pathways already reported in the literature for the classical chemistry in
Federico Cuccu +6 more
wiley +1 more source

