We describe the preparation and characterization of polythioesters composed of alternating alpha-amino acid and alpha-thioglycolic acid residues that undergo dynamic constitutional exchange under mild conditions. The polymers are assembled via reversible ring-opening polymerizations of 1,4-thiazine-2,5-diones and related monomers in solution-phase conditions that do not require the use of trans...

A series of known and newly synthesized pyrido-1,2-thiazine derivatives of type 3-6 were evaluated against strains of Mycobacterium fortuitum (PCM 672) and Staphylococcus aureus (PCM 2602) The pilot experiments showed that most of the compounds in initial in vitro microbiological evaluation were not efficient antibacterial agents, but unexpectedly promoted replication of the microorganisms in t...

The reaction of (Z)-2-amino-N′-arylbenzamidines 1, 2-amino-4,5,6,7-tetrahydrobenzo[b]-thiophene-3-carboxamide (4) and 4-amino-5-substituted-2-(phenylamino)thiophene-3-carboxamides 12 with o-phthalaldehyde (2), terephthalaldehyde (9), and 4-formyl[2.2]paracyclophane (16) in ethanol under reflux conditions afforded isoindoloquinazoline, thienopyrimidine, pyrimidine and thiazine derivatives, respe...

A catalytic atroposelective cycloaddition reaction between thioureas and ynals is developed. This features the first NHC-catalyzed addition of to acetylenic acylazolium intermediates eventually set up C?N axial chirality with excellent optical purities. The obtained axially chiral thiazine derivative products bear multiple functional groups are feasible for further transformations.

1,3-Thiazines are an important type of heterocycles showing a wide variety of pharmacological properties. Thus, 1,3-thiazine derivatives have recently been reported as cholecystokinin antagonists [1], antimycobacterial agents [2], cannabinoid receptor agonists [3], and inhibitors of NO synthase (NOS) [4], as antibacterial [5], antipyretic [6], anti-inflammatory [6, 7], analgesic [7], antitumor ...

acylisothiocyanate (1) was allowed to react with benzylidene malononitrile producing oxazine derivative (2). also, compound (1) was reacted with sodium azide followed by refluxing with sodium ethoxide affording thiazinotetrazole derivative (4). the reaction of acetylacetone with compound (1) gave pyridine derivative (5) by intramolecular cycloaddition while it was reacted with n-methyl aniline ...

A new synthetic approach to 2,3-dihydro-4H-1,3-thiazine derivatives based upon reductive rearrangement of 1,2-dithiole-3-ylidene thiones has been developed. In turn, the 1,2-dithiole derivatives were prepared by an efficient, ring-opening-closing process of 2-alkylidene-4-oxothiazolidines, induced in the presence of Lawesson’s reagent by intramolecular non-bonded 1,5-type S⋅⋅⋅O interactions in ...