Results 91 to 100 of about 4,651 (214)

Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine

open access: yes, 2017
4H-Dithieno[2,3-b:3’,2’-e][1,4]-thiazine (DTT), and its radical cation and dication were synthesized, characterized (EPR spectroscopy and spectroelectrochemistry) and interpreted (DFT and TD DFT calculations).
Guido J. Reiss   +5 more
core   +1 more source

On the significant influence of water on the formation mechanisms of 5-acetyl-3,4-dihydro-2H-1,4-thiazine

open access: yesCzech Journal of Food Sciences, 2004
The formation of 5-acetyl-3,4-dihydro-2H-1,4-thiazine in Maillard-type reactions of fructose with cysteamine under dry heating and cooking conditions was studied.
W. Engel, P. Schieberle
doaj   +1 more source

SYNTHESIS OF SUBSTITUTED BIS-THIAZINE DERIVATIVES OF IMINE COMPOUNDS AND ITS CHARACTERIZATION

open access: yes, 2017
The target compound bis-thiazine derivatives of imine were synthesized via three stages of chemical reaction. In a stage 1, a number of substituted chalcone derivatives were prepared by condensing with substituted aldehyde and acetophenone in the ...
M. Ganapathi, A. Ravi, R. Suganya
core   +1 more source

The synthesis of pyrrolo[1,2,b][1,2,5]benzothiadiazepines from 1,2-thiazine 1-oxides-sulfonamide analogues of the pyrrolobenzodiazepine antitumour natural products

open access: yes, 2004
Pyrrolo[2,1-c][1,4]benzodiazepines (PBDs) and the corresponding pyrrolobenzothiadiazepines (PBTDs) are attractive targets as natural and synthetic antitumour antibiotics and as non-nucleosidic reverse transcriptase inhibitors.
Patel, N., Hemming, Karl, Patel, Nilesh
core   +1 more source

(3R,5R)-TETRAHYDRO-2H-1,4-THIAZINE-3,5-DICARBOXYLIC ACID MONOHYDRATE

open access: yes, 1993
(3R,5R)-Tetrahydro-2H-1,4-thiazine-3,5-dicarboxylic acid monohydrate, which is in the zwitterionic form in the crystal, shows a puckered chair conformation of the six-membered ring with S(1) and N(4) out of the C(2), C(3), C(5), C(6) mean plane by 0.972 ...
PORTALONE G   +5 more
core   +1 more source

Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives

open access: yes, 2018
A highly efficient catalytic asymmetric [3 + 2] cycloaddition/rearrangement cascade of thiazolium N-ylides with various electron-deficient 2-π components was achieved, providing a convenient method to access hydropyrrolo-thiazole and hydropyrrolo ...
Dong Zhang   +5 more
core   +1 more source

Synthesis, Characterization, and Investigation of Biological Effects of Some New 1,2-Thiazine Derivatives

open access: yesZanco Journal of Pure and Applied Sciences
Nanomaterials and their applications hold a promise for widespread use in agriculture, medicine, and industry. This research article explores the synthesis of some new 1,2-thiazine derivatives, highlighting their potential as antibacterial agents.
Akram Noori Mohammed Qaddo   +8 more
doaj   +1 more source

Synthesis of 2--aryl--tetrahydro--3--methyl--4--H--1,3--thiazine--4--one--1,1--dioxides and chloromrthylation of p--dichloro-benzene [PDF]

open access: yes, 1966
Extensive background material and experimentation on the synthesis of 2--aryl--tetrahydro--3--methyl--4--H--1,3--thiazine--4--one--1,1--dioxides and chloromrthylation of p--dichloro ...
Downer, Robert Nye
core  

Direct Formation of Ring-Fused 1,3-Thiazine-2,4-dithiones from Aromatic o-Amino Carboxylic Acids: Observation of a Carbon Disulfide Mediated Thionation

open access: yes, 2016
A facile synthesis of 2H-3,1-benzothiazine-2,4(1H)-dithiones (trithioisatoic anhydrides) or 2H-naphtho[2,3-d][1,3]thiazine-2,4(1H)-dithione solely from anthranilic acids or 3-amino-2-naphthoic acid and carbon disulfide, performed at room temperature in 1,
Philipp A. Ottersbach (1734865)   +3 more
core   +1 more source

Three-dimensional structures of some perhydro-1,4-thiazine derivatives [PDF]

open access: yes, 1974
A number of perhydro-1,4-thiazine S-oxides and S,S-dioxides were synthesized. Their IR and PMR spectra were studied, and their dipole moments were determined.
Arbuzov B.   +3 more
core  

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