Results 1 to 10 of about 166 (105)
Synthesis and Antimicrobial Activity of 1,2-Benzothiazine Derivatives [PDF]
A number of 1,2-benzothiazines have been synthesized in a three-step process. Nine chalcones 1–9 bearing methyl, fluoro, chloro and bromo substituents were chlorosulfonated with chlorosulfonic acid to generate the chalcone sulfonyl chlorides 10–18. These
Chandani Patel +6 more
doaj +12 more sources
Methyl 4-ethoxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide [PDF]
In the crystal structure of the title compound, C13H15NO5S, the molecules exhibit weak S=O...H—C and C=O...H—C intermolecular interactions and arrange themselves into centrosymmetric dimers by means of π–π interactions (ring ...
Muhammad Zia-ur-Rehman +4 more
doaj +3 more sources
N-(3,4-Dimethylphenyl)-4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide [PDF]
1,2-Benzothiazines similar to the title compound, C18H18N2O4S, are well known in the literature for their biological activities and are used as medicines in the treatment of inflammation and rheumatoid arthritis. The thiazine ring adopts a distorted half-
Waseeq Ahmad Siddiqui +4 more
doaj +2 more sources
Sulfoximines-Assisted Rh(III)-Catalyzed C–H Activation and Intramolecular Annulation for the Synthesis of Fused Isochromeno-1,2-Benzothiazines Scaffolds under Room Temperature [PDF]
A mild and facile Cp*Rh(III)-catalyzed C–H activation and intramolecular cascade annulation protocol has been proposed for the furnishing of highly fused isochromeno-1,2-benzothiazines scaffolds using S-phenylsulfoximides and 4-diazoisochroman-3-imine as
Bao Wang +4 more
doaj +3 more sources
In this study, we report the synthesis of unsubstituted 1,2-benzothiazines through a redox-neutral Rh(III)-catalyzed C–H activation and [4+2]-annulation of S–aryl sulfoximines with vinylene carbonate.
Koneti Kondalarao +2 more
doaj +2 more sources
The global concern related with growing number of bacterial pathogens, resistant to numerous antibiotics, prone scientific environment to search for new antimicrobials.
Ruth K. Dudek-Wicher +5 more
doaj +2 more sources
Taking advantage of facilely available α-chloroketones as C(sp3)-based electrophilic partners and oxidized alkyne equivalents, we here present a novel CpxRh(III)-catalyzed enantioselective C–H [4 + 2] annulation of sulfoximines under mild and redox ...
Qingwei Song +6 more
doaj +2 more sources
Synthesis of 1,2-Benzothiazines via C–H Activation/Cyclization in a Recyclable, Mild System
A mild and recyclable protocol to synthesize 1,2-benzothiazines by Rh(III)-catalyzed C–H activation/cyclization of NH-sulfoximines in ionic liquids with high yields is described.
Li Hai, Yong Wu
exaly +2 more sources
In this study, a modular approach toward cyclic sulfoximines and sulfondiimines via palladium-catalyzed intramolecular C–H/C-C activation reactions was reported.
Fan Teng (1581460) +7 more
core +3 more sources
THE SYNTHESIS OF SOME NEW 1,2-BENZOTHIAZINES [PDF]
Joseph G. Lombardino
core +2 more sources

