WebSep 3, 2009 · The synthesis of several hitherto unknown heterocyclic ring systems derived from thioflavone is described. Coupling of various o-haloheteroarenecarbonyl chlorides with phenylacetylene gives 1-(o-haloheteroaryl)-3-phenylprop-2-yn-1-ones, which were treated with NaSH in refluxing ethanol to yield the corresponding bi- and tricyclic annelated 2 … WebA copper-catalyzed intramolecular ring opening of donor-acceptor cyclopropanes in the presence of xanthate as a sulfur surrogate enables the synthesis of 3-alkyl-carbonated thioflavones and 3-alkyl-carbonated thioflavothiones. N. Sundaravelu, G. Sekar, Org. Lett., 2024, 21, 6648-6652. A mild ICl-induced cyclization of heteroatom-substituted ...
Molecules Free Full-Text Heterocyclic Analogs of Thioflavones ...
WebApr 2, 2024 · ABSTRACT 3-CF3S substituted thioflavones and benzothiophenes were achieved via the reactions of AgSCF3 with methylthiolated alkynones and alkynylthioanisoles, respectively, promoted by persulfate.This protocol possesses good functional group tolerance and high yields.Mechanistic studies suggested that a classic … WebJun 8, 2024 · A new and efficient approach for the synthesis of thioflavones and thioaurones by competitive cascade cyclization of 2′-tosyloxychalcones has been developed. 2′-Tosyloxychalcones were smoothly converted into thioflavones and thioaurones by incorporation of sulfur atom using elemental sulfur and triethylamine in … flowers bergen county nj
Visible‐Light‐Induced Metal‐Free Synthesis of …
WebThioflavones are an important class of sulfur-containing heterocycles in medicinal chemistry due to their structural similarity to flavones, and this scaffold exhibits various biological and pharmacological properties, including antibacterial, anticancer, and anti-HIV activities. However, the synthetic methods for thioflavones via cross-coupling reaction are … WebIsoflavone is an isomer of flavone, which is chromone substituted with a phenyl group in the 2-position. In isoflavone, the phenyl group is in the 4-position. [4] Substituted isoflavone … WebA set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions. The features of this procedure included metal-free reaction cond green and wilds antler