A decade update on the application of β-oxodithioesters in heterocyclic synthesis
ZB Dong, Z Gong, Q Dou, B Cheng… - Organic & Biomolecular …, 2023 - pubs.rsc.org
The diversified synthesis of heterocyclic compounds has always been one of the popular
subjects of organic chemistry. To this end, great efforts have been devoted to developing …
subjects of organic chemistry. To this end, great efforts have been devoted to developing …
Catalyst-free one-pot four-component domino reactions in water–PEG-400: Highly efficient and convergent approach to thiazoloquinoline scaffolds
A cost-effective and eco-friendly straightforward synthesis of highly diversified
thiazoloquinoline scaffolds is successfully achieved via one-pot four-component cascade …
thiazoloquinoline scaffolds is successfully achieved via one-pot four-component cascade …
Facile one-pot, multi-component reaction to synthesize spirooxindole-annulated thiopyran derivatives under environmentally benevolent conditions
FM Moghaddam, B Aghamiri - Heliyon, 2022 - cell.com
An efficient and facile one-pot, five-component reaction for the synthesis of 2, 6-diamino-1-
alkyl-2-oxospiro [indoline-3, 4′-thiopyran]-3, 5-dicarbonitrile derivatives has been reported …
alkyl-2-oxospiro [indoline-3, 4′-thiopyran]-3, 5-dicarbonitrile derivatives has been reported …
A facile one-pot, three component synthesis of a new series of 1, 3, 4-thiadiazines: Anticancer evaluation and molecular docking studies
S Mamidala, V Vangala, SR Peddi… - Journal of Molecular …, 2021 - Elsevier
Abstract A series of new 1, 3, 4-thiadiazines were synthesized by the conventional method of
dehydroacetic acid, thiocarbohydrazide and substituted phenacyl bromides or substituted 3 …
dehydroacetic acid, thiocarbohydrazide and substituted phenacyl bromides or substituted 3 …
Two Different Green Catalytic Systems for One‐Pot Regioselective and Chemoselective Synthesis of Some Pyrimido[4,5‐d]Pyrimidinone Derivatives in Water
In this work, we have developed green and efficient regioselective and chemoselective
syntheses of 5‐aryloyl‐1, 3‐dimethyl‐7‐thioxo‐5, 6, 7, 8‐tetrahydropyrimido [4, 5‐d] …
syntheses of 5‐aryloyl‐1, 3‐dimethyl‐7‐thioxo‐5, 6, 7, 8‐tetrahydropyrimido [4, 5‐d] …
A facile one-pot, three-component synthesis of a new series of thiazolyl pyrazole carbaldehydes: In vitro anticancer evaluation, in silico ADME/T, and molecular …
A series of thiazolyl pyrazole carbaldehydes (4a-n) were synthesized by conventional
method using thiosemicarbazide, substituted phenacyl bromides, substituted 3 …
method using thiosemicarbazide, substituted phenacyl bromides, substituted 3 …
CuSO 4–d-glucose, an inexpensive and eco-efficient catalytic system: direct access to diverse quinolines through modified Friedländer approach involving SN Ar …
A highly efficient and scalable multicomponent domino reaction for the synthesis of
functionalized/annulated quinolines is devised directly from 2-bromoaromatic …
functionalized/annulated quinolines is devised directly from 2-bromoaromatic …
Multicomponent Reactions in the Last 30 Years: How are we Today?
In this review, the works carried out in Brazil with multicomponent reactions over a period of
30 years were mapped through search in the literature (PubMed, Scopus, and Web of …
30 years were mapped through search in the literature (PubMed, Scopus, and Web of …
Magnesium catalyzed [3+ 3] heteroannulation of α-enolic dithioesters with MBH acetate: access to functionalized 3, 4-dihydro-2 H-thiopyrans
Magnesium catalysis proved to be efficient towards [3+ 3] chemo-and diastereoselective
heteroannulation employing racemic Morita–Baylis–Hillman (MBH) acetate as the C3 unit …
heteroannulation employing racemic Morita–Baylis–Hillman (MBH) acetate as the C3 unit …
Regioselective dehydrative intramolecular heteroannulation of β-allyl-β-hydroxy dithioesters: facile and straightforward entry to 2H-thiopyrans
Abstract β-Allyl-β-hydroxy dithioesters have been employed in the synthesis of hitherto
unreported and synthetically demanding 2 H-thiopyrans via regioselective intramolecular …
unreported and synthetically demanding 2 H-thiopyrans via regioselective intramolecular …