Results 31 to 40 of about 806 (175)

Synthesis and Structure of Novel 1λ4,2,6-Thiadiazines

open access: yes, 2016
S,S-Disubstituted sulfodiimines 9 are known to be versatile building blocks for the synthesis of various sulfur−nitrogen-containing heterocycles. Addition−condensation reactions of 9 with three different activated carbonylsubstrates 14−16 lead to several
Manfred Haake (3034236)   +1 more
core   +1 more source

Synthesis and Biological Activity of Some Novel Derivatives of 4-Amino-3-(D-galactopentitol-1-yl)-5-mercapto-1,2,4-triazole

open access: yesMolecules, 2007
To discover new 1,2,4-triazole derivatives which may possess significant biological activities, we synthesized a series of novel 6-aryl-3-(D-galactopentitol-1-yl)- 7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazines and 4-(arylmethylidene)amino-5-(D ...
Jiang-Hai Zhu   +4 more
doaj   +1 more source

Impact of Tetrahydropyrido[2,1-b][1,3,5]thiadiazines on L-DOPA Effects in the Tail Suspension Test

open access: yesКубанский научный медицинский вестник, 2020
Aim. Evaluation of the impact of tetrahydropyrido[2,1-b][1,3,5]thiadiazine derivatives on L-DOPA effects in the tail suspension test.Materials and methods.
E. Yu. Bibik   +6 more
doaj   +1 more source

3-Chloro-5-(4-dodecylthiophen-2-yl)-4H-1,2,6-thiadiazin-4-one

open access: yesMolbank, 2012
3-Chloro-5-trifluoromethanesulfonate-4H-1,2,6-thiadiazin-4-one 3 reacts with (4-dodecylthiophen-2-yl)trimethylstannane 5 (1 equiv.) in the presence of Pd(Ph3P)2Cl2 (5 mol%) in benzene at ca.
Panayiotis A. Koutentis   +1 more
doaj   +1 more source

Effects of a compound from the group of substituted thiadiazines with hypothermia inducing properties on brain metabolism in rats, a study in vivo and in vitro. [PDF]

open access: yesPLoS ONE, 2017
The aim of the present study was to examine how administration of a compound of 1,3,4- thiadiazine class 2-morpholino-5-phenyl-6H-1,3,4-thiadiazine, hydrobromide (L-17) with hypothermia inducing properties affects the brain metabolism.
O B Shevelev   +5 more
doaj   +1 more source

Design, Synthesis, and Antimicrobial Evaluation of Novel Pyrazoles and Pyrazolyl 1,3,4-Thiadiazine Derivatives

open access: yesMolecules, 2018
A novel series of pyrazolyl 1,3,4-thiadiazines 5a–c, 8a–c, 12, 15a–c, 17a–c, and 20 was prepared from the reaction of pyrazole-1-carbothiohydrazide 1a,b with 2-oxo-N′-arylpropanehydrazonoyl chloride, 2-chloro-2-(2 ...
Ibrahim Ali M. Radini
doaj   +1 more source

Substituted 2-amino-1,3,4-thiadiazines: a novel solid-phase approach

open access: yes, 2002
A novel and facile strategy for synthesis of substituted 2-amino-1,3,4-thiadiazines on solid support is described. Resin bound isothiocyanate prepared from an immobilised primary amine and di-(2-pyridyl)thionocarbonate was reacted with hydrazine hydrate ...
Jones, Raymond C. F.   +2 more
core   +1 more source

An Improved Synthesis of 4-Chlorocoumarin-3-sulfonyl Chloride and Its Reactions with Different Bidentate Nucleophiles to Give Pyrido[1',2':2,3]- and Thiazino[3',2':2,3]-1,2,4-Thiadiazino[6,5-c]Benzopyran-6-one 7,7-Dioxides

open access: yesMolecules, 2007
An improved synthetic method affording 4-chlorocoumarin-3-sulfonyl chloride (4) in very good yield (ca. 85 %) is reported. This compound was reacted with various bidentate nucleophiles such as 2-aminopyridines and 2-aminothiazoles in order to obtain ...
Emil Popovski   +4 more
doaj   +1 more source

The Photochemical Mediated Ring Contraction of 4H‑1,2,6-Thiadiazines To Afford 1,2,5-Thiadiazol-3(2H)‑one 1‑Oxides

open access: yes, 2023
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%).
Emmanouil Broumidis   +25 more
core   +1 more source

The Mannich Reaction of the S,N-Binucleophilic Species Derived from Meldrum’s Acid with HCHO and Primary Amines

open access: yesChemistry Proceedings
We investigated the reactivity of a new sulfur-containing compound derived from Meldrum’s acid and phenyl isothiocyanate, triethylammonium 1-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)(phenylamino)methanethiolate.
Anastasiya Yu. Skachkova   +2 more
doaj   +1 more source

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