A REVIEW: THIAZINES DERIVATIVES TREATED AS POTENTIAL ANTIMICROBIAL AGENTS [PDF]
In recent days, heterocycles and their derivatives have become strong reflection in medicinal research and pharmaceutical fields because of their practical pharmacological and biological activities.
Makkar, Reena, Sharma, Praveen Kumar
core +1 more source
Thiazine; Synthesis and Biological Activity
Thiazines are a class of heterocyclic molecules that have not been extensively studied for their pharmacological effects. Various methods for synthesizing thiazine derivatives can be found in the literature. This review examines various techniques for synthesizing thiazines using environmentally friendly approaches. Thiazine derivatives are synthesized
ASMAA Jawad, Tamam Mahdi Salih
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REACTION OF ETHYL 3-AMINOTHIENO[2,3-B]PYRIDINE-2-CARBOXYLATE: SYNTHESIS OF NEW FUNCTIONALIZED THIENO[2,3-B]PYRIDINE, PYRIDO[3',2':4,5]THIENO[3,2-D][1,3]THIAZINE AND PYRIDO[3',2':4,5]THIENO[3,2-D]PYRIMIDINES [PDF]
Mehdi Bakavolia +4 more
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Alternative Synthesis of 2,4-Substituted-1,3-thiazines and 2,5-Substituted-thiazole Derivatives [PDF]
Aneasy and convenient route for the synthesis of 2,4-substituted thiazine (3–6) and 2,5-substituted thiazole (16) derivatives from phenacetamidines and glycine methyl ester is reported.
Bisetty, K, Mahajan, MP, Singh, P
core +1 more source
Visible light responsive titanium dioxide (TiO
Titanium dioxide (TiO2) is one of the most researched semiconductor oxides that has revolutionised technologies in the field of environmental purification and energy generation.
Cho, DL +8 more
core
Generation and reactions of thionitroso and thioxophosphine intermediates [PDF]
A series of alkylthionitroso compounds have been generated via thermal fragmentation of N-chlorothio-N-trimethylsilylalkylamines and intercepted with dienes to form 1,2-thiazine heterocycles (via Diels-Alder reaction) and N-alkylsulfenamides (via Ene ...
Mckelvey, Graham Neil
core
Zur Kenntniss der Thiazine [PDF]
R. Gnehm, F. Kaufler
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New Insight into Dearomatization and Decarbonylation of Antitubercular 4H-Benzo[e][1,3]thiazinones: Stable 5H- and 7H-Benzo[e][1,3]thiazines. [PDF]
Richter A +7 more
europepmc +1 more source

