Results 21 to 30 of about 1,673 (99)
3,5-Bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one
Stille coupling of 3,5-bis(5-bromothien-2-yl)-4H-1,2,6-thiadiazin-4-one (10) with 2-(tri-n-butylstannyl)thiazole and Pd(Ph3P)2Cl2 in PhMe, at ca. 110 °C, for 2 h, gave 3,5-bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one (9) in 81% yield.
Andreas S. Kalogirou +1 more
doaj +2 more sources
2-[3,5-Bis(5-bromothien-2-yl)-4H-1,2,6-thiadiazin-4-ylidene]-malononitrile
Bromination of 2-[3,5-di(thien-2-yl)-4H-1,2,6-thiadiazin-4-ylidene]-malononitrile with N-bromosuccinimide in THF, at ca. 20 °C for 24 h gave 2-[3,5-bis(5-bromothien-2-yl)-4H-1,2,6-thiadiazin-4-ylidene]-malononitrile in 82% yield.
Andreas S. Kalogirou +2 more
doaj +2 more sources
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
Oxidations of 4H‐1,2,6‐Thiadiazines
The oxidation of various non‐S‐oxidized 4H‐1,2,6‐thiadiazines to sulfoxides and sulfones was investigated using the oxidants N2O4, m‐CPBA, Oxone, PIFA and PIDA. The scope and regioselectivity of the oxidation was examined, while the structures of several new products is supported by X‐ray crystallography.
Andreas S. Kalogirou +2 more
wiley +1 more source
1,2,6-Thiadiazine 1-Oxides : Unsaturated Three-Dimensional S,N-Heterocycles from Sulfonimidamides
Unprecedented three-dimensional 1,2,6-thiadiazine 1-oxides have been prepared by an aza-Michael-addition/cyclization/condensation reaction sequence starting from sulfonimidamides and propargyl ketones.
Wolter, Nadja Anna +5 more
core +2 more sources
The title compound, C15H22N4O5S, was prepared via alkylation of 3-(chloromethyl)-5-(pentan-3-yl)-1,2,4-oxadiazole in anhydrous dioxane in the presence of triethylamine. The thiadiazine ring has an envelope conformation with the S atom displaced by 0.4883
Alexandre V. Ivachtchenko +5 more
doaj +1 more source
5 pags., 3 figs., 8 tbs.In a previous paper (1) we carried out a comparative study between the physicochemical properties of 1,2,6-thiadiazine 1,l-dioxide derivatives and related pyrazoles.
Ochoa, Carmen +5 more
core +1 more source
Reactions of 3′,5′-dichlorospiro(benzo[d][1,3]dioxole-2,4′-[1,2,6]thiadiazine) or 6,10-dichloro-1,4-dioxa-8-thia-7,9-diazaspiro[4.5]deca-6,9-diene with ammonia in MeCN, at ca.
Andreas S. Kalogirou +1 more
doaj +1 more source
Selective procedures for the synthesis of 6- and of 7-monosubstituted derivatives of pyrazinoI2,3-c̱|-1 ,2,6- thiadiazine 2,2-dioxide and their reactions with N-bromosuccinimide are reported.
Alkorta Ibon +3 more
doaj +1 more source
A 4H-1,2,6-thiadiazine motif as a new acceptor for D–A conjugated polymers.
Vasilis G. Gregoriou +8 more
core +1 more source

