Safety of 3,5-Dimethyl-1H-pyrazole. I found the field of Chemistry very interesting. Saw the article Pd-Catalyzed Asymmetric Dearomatization of Indoles via Decarbonylative Heck-Type Reaction of Thioesters published in 2021.0, Reprint Addresses Xiong, H (corresponding author), Shenzhen Univ, Inst Adv Study, Coll Optoelect Engn, Shenzhen 518060, Peoples R China.; Xiong, H (corresponding author), Shenzhen Univ, Key Lab Optoelect Devices & Syst, Coll Optoelect Engn, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China.; Xu, H; Dai, HX (corresponding author), Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Shanghai 201203, Peoples R China.. The CAS is 67-51-6. Through research, I have a further understanding and discovery of 3,5-Dimethyl-1H-pyrazole.
We report herein a palladium-catalyzed ligand-promoted asymmetric dearomatization of indoles via the decarbonylation of thioesters and the subsequent reductive Heck reaction. This protocol provides a facile and efficient way to construct an aza-quaternary stereocenter at the C2 position of indolines. A variety of functional groups and substitutions could be well tolerated, affording the substituted indolines with high enantioselectivities.
About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Han, ML; Huang, W; Liu, YW; Liu, M; Xu, H; Xiong, H; Dai, HX or concate me.. Safety of 3,5-Dimethyl-1H-pyrazole
Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics