An article Access to Sulfides through Free Radical Reaction of Vinyl Halides with Thiols WOS:000456244000024 published article about CROSS-COUPLING REACTIONS; ALKENYL SULFIDES; C-S; HYDROTHIOLATION; PALLADIUM; EFFICIENT; CATALYST; KETONES; ALKYNES; LIGAND in [Shi, Zi-Fa; Xu, Li-Ning; Chen, Jie; Luo, Hui-Xing; Zhang, Juntao; Cao, Xiao-Ping] Lanzhou Univ, State Key Lab Appl Organ Chem, 222 Tianshui Rd, Lanzhou 730000, Gansu, Peoples R China; [Shi, Zi-Fa; Xu, Li-Ning; Chen, Jie; Luo, Hui-Xing; Zhang, Juntao; Cao, Xiao-Ping] Lanzhou Univ, Coll Chem & Chem Engn, 222 Tianshui Rd, Lanzhou 730000, Gansu, Peoples R China in 2019.0, Cited 56.0. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6
An efficient radical-mediated carbon-sulfur bond formation reaction of vinyl halides with thiols has been developed. This reaction tolerated vinyl chloride substrates, which are barely tolerated in metal-catalyzed reactions, providing vinyl sulfide products. When vinyl iodides were used as substrates, the reactions were regulated by the solvents, yielding vinyl sulfide products in protic solvents (methanol) and alkyl sulfides in aprotic solvents (toluene).
Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Shi, ZF; Xu, LN; Chen, J; Luo, HX; Zhang, JT; Cao, XP or concate me.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem