Sulfonoketenimides as key intermediates for the synthesis of 2-thioxo-2HH-1,3-thiazines and 2-arylimino-2HH-1,3-thiazines
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Summary
Using isothiocyanates as the heterocumulene component, affords 2-arylimino-1,3-thiazine derivatives in moderate to good yields.
- Type
- article
- Published
- 2013-09-20
- Cited by
- 24
- References
- 37
- OpenAlex
- https://openalex.org/W307091661
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:2268883
Keywords
Key (lock), Chemistry, Combinatorial chemistry, Medicinal chemistry, Computer science
References
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- A synthesis of phosphorylated dioxohexahydropyrimidines from N,N′-dimethylurea, activated acetylenes, and trialkyl phosphites
Cited by
- A tandem synthesis of 5-sulfonylimino-2-imidazolones from sulfonoketenimides and dialkyl azodicarboxylates
- An efficient synthesis of phenylcarbamimidic (thio)anhydride derivatives containing a sulfonyl moiety
- A green, synthesis of spiro-indene-2,6′-thiazines from tetramethylguanidine-heterocumulene and ninhydrin-malononitrile adducts
- An efficient synthesis of novel sulfonyl[3.3.3]heteropropellanes from sulfonylacetamidines and ninhydrin-malononitrile adduct
- A synthesis of oxo-thioxo[3.3.3]propellanes from dithiocarbamates and ninhydrin–malononitrile adduct
- A synthesis of functionalized arylthio-acrylates, benzo[b][1,4]thiazines and benzo[4,5]thiazolo[3,2-a]azepines from 2-methylbenzothiazole and acetylenic esters in aqueous media
- A Novel One-pot Protocol for the Cu-Catalyzed Synthesis of Nine 2-Aminobenzimidazole Derivatives from o-Phenylenediamine and Trichloroacetonitrile
- One‐pot synthesis of highly functionalized benzo [1,3] thiazine from isocyanides, aniline, and heterocumulene via Cu‐catalyzed intramolecular C‐H activation reactions
- Synthesis of poly-substituted thiophenes in the realm of sulfonylketenimines chemistry
- N-sulfonyl ketenimine as a versatile intermediate for the synthesis of heteroatom containing compounds
- Formation of quinazolin-4(3H)-ones from N-sulfonoketenimines and 2-aminobenzamides
- Convenient synthesis of highly functionalized isoxazoles including an amidine skeleton based on trichloroacetamidine, alkynes, and hydroxyimidoyl chloride
- Convenient synthesis of multi-substituted isoxazoles including a sulfonamide skeleton based on N-sulfonylketenimine and hydroxyimidoyl chloride
- Cu-Catalyzed Synthesis of Isoxazolidine/1,2-Oxazinane-3-ylidene Sulfonamide from O-Alkynyl Hydroxylamines: A Route to Sulfamethoxazole Analogues.
- Efficient Synthetic Strategies for Highly Functionalized Pyrazole Including an Amidine Skeleton Based on Trichloroacetamidine, Alkynes, and Hydrazonoyl Chlorides
- Domino reaction for the synthesis of new highly functionalized pyridine derivatives from alkynes, trichloroacetamidine(imidate), and 2-amino-1,1,3-tricyanopropylene
- Tandem synthesis of novel substituted sulfonyl-imino-sulfonamide derivatives from terminal alkynes, sulfonyl azides, isocyanide, and sodium arylsulfinates under ultrasound irradiation
- Innovative ultrasound‐assisted synthesis of new highly functionalized pyrroles derivatives from alkynes, trichloroacet-amidine(imidate), and nitro compounds-trichloroacetonitrile adducts
- Synthesis of new 2-(thiazol-2-ylidene) malononitrile, and 2-(1,3-selenazol-2-ylidene) malononitrile derivatives via nitroepoxide ring opening with malononitrile-isothiocyanate (or isoselenocyanate) adducts
- Catalyst free, three components synthesis of new 2-(1,3-dithiol-2-ylidene)malononitrile and 2-(thiazol-2-ylidene)malononitrile from nitroepoxides and malononitrile-heterocumulene adducts
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