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

open access: yesMolbank, 2019
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

open access: yesMolbank
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

open access: yesChemistrySelect, Volume 8, Issue 45, December 5, 2023., 2023
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

open access: yesChemistrySelect, Volume 7, Issue 45, December 6, 2022., 2022
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

open access: yes, 2020
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

Crystal structure, Hirshfeld analysis and a molecular docking study of a new inhibitor of the Hepatitis B virus (HBV): ethyl 5-methyl-1,1-dioxo-2-{[5-(pentan-3-yl)-1,2,4-oxadiazol-3-yl]methyl}-2H-1,2,6-thiadiazine-4-carboxylate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2020
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

1,2,6-Thiadiazin-3,5(2H,6H)-dione 1,1-dioxide derivatives: crystal structure, physico-chemical and biological properties

open access: yes, 2022
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

Synthesis of 5′-Chlorospiro(benzo[d][1,3]dioxole-2,4′-[1,2,6]thiadiazin)-3′-amine and 10-Chloro-1,4-dioxa-8-thia-7,9-diazaspiro[4.5]deca-6,9-dien-6-amine

open access: yesMolbank
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

Synthesis and Physico-Chemical Properties of 6- and 7-Monosubstituted Pyrazino|2,3-c̱|-1,2,6-thiadiazine 2,2-Dioxides

open access: yesPteridines, 1990
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

4H-1,2,6-Thiadiazine-containing donor–acceptor conjugated polymers: synthesis, optoelectronic characterization and their use in organic solar cells

open access: yes, 2018
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

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