External oxidant-free and selective thiofunctionalization of alkenes enabled by photoredox-neutral catalysis was written by Liang, Rong-Bin;Zhu, Can-Ming;Song, Pei-Qi;Zhao, Lei-Min;Tong, Qing-Xiao;Zhong, Jian-Ji. And the article was included in Organic Chemistry Frontiers in 2022.COA of Formula: C14H9NO2S This article mentions the following:
A simple photoredox-neutral approach is reported for the three-component thiohydroxylation, thioalkoxylation and thioamination of vinylarenes ArC(R)=CH2 (Ar = Ph, 3-bromophenyl, 2H-1,3-benzodioxol-5-yl, etc.; R = H, Me, Ph, thien-2-yl, etc.) towards valuable vicinal S,O- and S,N-disubstituted mols. N-Phenyl-sulfenyl phthalimides I (R1 = Ph, 2-chlorophenyl, naphthalen-2-yl, etc.), a commonly used sulfur electrophile, were demonstrated to act as a thiyl radical precursor and play a crucial role in this reaction. In the experiment, the researchers used many compounds, for example, 2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4COA of Formula: C14H9NO2S).
2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.COA of Formula: C14H9NO2S
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles