Results 51 to 60 of about 6,902 (250)
Crystal structure of methyl 1-allyl-4-methyl-1H-benzo[c][1,2]thiazine-3-carboxylate 2,2-dioxide
In the title compound, C14H15NO4S, the dihydrothiazine ring adopts a distorted sofa conformation with the S atom displaced from the mean plane through the N and C ring atoms by 0.767 (1) Å.
Liliana Azotla-Cruz +4 more
doaj +1 more source
(Z)-4-n-Butyl-2-(4-chlorobenzylidene)-2H-1,4-benzothiazin-3(4H)-one
In the title compound, C19H18ClNOS, the thiazin-3-one ring adopts a slightly distorted screw-boat conformation. An intramolecular C—H...S hydrogen bond encloses an S(6) ring and affects the overall conformation of the molecule. The dihedral angle between
Mohamed Ellouz +5 more
doaj +1 more source
ABSTRACT The objective of this in vitro experimental was to determine the utility of hemoadsorption (HA) using the CytoSorb adsorber to remove meloxicam and diclofenac from porcine plasma. For this purpose 12 1‐L aliquots of porcine plasma, 6 units were spiked with 293 μg/mL (262–320 μg/mL) diclofenac and 6 with 42.8 μg/mL (41.4–44.7 μg/mL) meloxicam ...
Bettina Giani +3 more
wiley +1 more source
Crystal structures of methyl 2-pentyl-4-hydroxy-2H-1,2-benzothiazine-3-carboxylate-1,1-dioxide 1 and methyl 2-pentenyl-4-hydroxy-2H-1,2-benzothiazine-3-carboxylate-1,1-dioxide 2 have been determined after their synthesis from saccharin.
Muhammad Nadeem ARSHAD +6 more
doaj +1 more source
Experimental and quantum chemical calculations on corrosion inhibition of mild steel by two furan derivatives [PDF]
Two furan derivatives namely 5-methylfurfurylamine (MFA) and furfurylamine (FAM) were investigated as corrosion inhibitors for mild steel in 1 M HCl.
Abdallah, H. H. +3 more
core +1 more source
Sulfoximine directed C-H activation strategy catalyzed by Rh-catalyst leads to an efficient synthesis of furanone fused 1,2-benzothiazine. In this reaction, cascade C-H activation, regioselective annulations, and lactonization, occur in one-pot.
Vinayak Hanchate +2 more
semanticscholar +1 more source
Benzothiazines in Synthesis. A Total Synthesis of Pseudopteroxazole. [PDF]
An enantioselective total synthesis of the naturally occurring antitubercular agent pseudopteroxazole is described. The synthesis is organized around the use of a stereoselective, intramolecular addition of a sulfoximine carbanion to an alpha,beta-unsaturated ester to form an enantiomerically pure benzothiazine.
Michael, Harmata, Xuechuan, Hong
openaire +2 more sources
Synthesis of Sulfur Heterocycles by Palladium‐Catalyzed Cyclization
In spite of the well‐known palladium thiophilicity, sulfur‐containing acyclic substrates may efficiently undergo several different kinds of palladium‐catalyzed cyclization processes leading to highly important sulfur heterocycles in one synthetic step. Advances in this challenging and stimulating field of research are presented in this review.
Bartolo Gabriele
wiley +1 more source
Herein, we develop a novel SAM molecular design strategy by introducing fused‐ring intramolecular donor–acceptor (D–A) interactions. The designed molecule, JJ32, features a benzo[5,6][1,4]thiazino[2,3‐b]quinoxaline skeleton, where strong D–A interactions enhance charge delocalization and downshift the LUMO energy level.
Wenlin Jiang +7 more
wiley +2 more sources
Proteome‐Wide Analysis of Cysteine S‐Sulfenylation Using a Benzothiazine‐Based Probe
Oxidation of a protein cysteinyl thiol (Cys‐SH) to S‐sulfenic acid (Cys‐SOH) by a reactive oxygen species (e.g., hydrogen peroxide), which is termed protein S‐sulfenylation, is a reversible post‐translational modification that plays a crucial role in ...
L. Fu +4 more
semanticscholar +1 more source

