Results 1 to 10 of about 1,925 (186)

Green Synthesis of 2-Mercapto 5,6-Dihydro-4H-1,3-Thiazines via Sequential C–S Couplings [PDF]

open access: yesMolecules
The six-membered N,S-heterocyclic 1,3-thiazines and their derivatives are widely acknowledged as pharmaceutical molecules with a wide range of biological activities.
Wenjie Liu   +4 more
doaj   +2 more sources

Synthesis, characterization, and DFT study of a novel pyrido[2',3':4,5]pyrimido[2,1-b][1,3]thiazines via Michael addition and intramolecular cyclization [PDF]

open access: yesBMC Chemistry
Two novel series of pyrido[2',3':4,5]pyrimido[2,1-b][1,3]thiazine-3-carbonitriles and ethyl pyrido[2',3':4,5]pyrimido[2,1-b][1,3]thiazine-3-carboxylates were synthesized from a key intermediate 2-thioxo-2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-one via its
Bader Huwaimel   +9 more
doaj   +2 more sources

Facile Synthesis of Some Novel Pyrido[3', 2': 4, 5]thieno[2,3-b][1,4]thiazine-8-carboxylic Acids

open access: yesMolecules, 2007
Model tetrahydropyrido[3',2':4,5]thieno[2,3-b][1,4]thiazines 9a-c were synthesized via reductive lactamization, using sodium dithionite, of the respective 2-[(carboxyalkyl)thio]-3-nitro-4,7-dihydrothieno[2,3-b]pyridine-5-carboxylic acids 7a-c. The latter
Salim S Sabri   +4 more
doaj   +1 more source

Methyl (1aRS,7aSR)-7-formyl-1a-phenyl-1,1a-dihydroazirino[2,3-b]benzo[e][1,4]thiazine-7a(7H)-carboxylate

open access: yesMolbank
The first representative of the aziridine-fused benzo[e][1,4]thiazine series was synthesized from methyl 2-bromo-2-phenyl-2H-azirine-2-carboxylate and benzo[d]thiazole in 74% yield.
Ilya P. Filippov   +3 more
doaj   +1 more source

A rapid and effective catalytic pathway for the synthesis of thiazine derivatives employing Zno nanoparticles

open access: yesEnvironment Conservation Journal
A sustainable approach has been successfully developed for the synthesis of thiazine derivatives, utilizing an efficient catalytic method. ZnO nanoparticles have demonstrated remarkable catalytic prowess, offering cost-effectiveness, heightened yields ...
Raksha Parag Dhankar   +2 more
doaj   +1 more source

On the functionalization of benzo[e][2,1]thiazine [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2009
The reactions of benzo[e][2,1]thiazine-4-chloro-3-carbaldehydes1and benzo[e][2,1]thiazine-4-chloro-3-carbonitriles2with a number of oxidizing and reducing agents are reported. A number of new, highly functionalized benzo[e][2,1]thiazine derivatives having potential biological activity were synthesized and described.
Kirill Popov   +2 more
openaire   +3 more sources

Comparison of dye (oxazine and thiazine) materials as a photosensitizer for use in photogalvanic cells based on molecular interaction with sodium dodecyl sulphate by spectral study

open access: yesJournal of Saudi Chemical Society, 2018
The photochemistry of dye is playing a significant role for understanding the mechanism of electron transfer reactions in photoelectrochemical devices such as photogalvanic cells, DSSC, semiconductor photo-catalysis, photoconductors, etc.
Chandrakanta Mall   +2 more
doaj   +1 more source

2,3-Dihydro-5H-imidazo [2,1-b][1,3]thiazin-5-one

open access: yesMolbank
Imidazo [2,1-b][1,3]thiazines and their fused analogues are an important class of nitrogen- and sulfur-containing heterocycles that exhibit a wide range of biological activities.
Nataliia Slyvka   +4 more
doaj   +1 more source

Design, evaluation, cytotoxic activity, molecular docking, ADMET analysis, and dynamic simulations and the preparation of new isoxazoles, thiazoles, 1,3-thiazines, and thiazolopyrimidines derived from quinoline-pyridopyrimidines

open access: yesPharmaceutical Biology
Context Quinoline, isoxazole, and pyridothiazolopyrimidinone derivatives are novel compounds with significant biological activity, exhibiting anticancer properties and holding promising therapeutic applications.Objective This investigation synthesized ...
Ameen A. Abu-Hashem   +2 more
doaj   +1 more source

Zur Kenntniss der Thiazine [PDF]

open access: yesBerichte der deutschen chemischen Gesellschaft, 1906
n ...
Gnehm, R., Kaufler, F.
openaire   +1 more source

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