In 2020.0 J ORG CHEM published article about METAL-FREE HYDROGENATION; ASYMMETRIC CONJUGATE REDUCTION; CROSS-COUPLING REACTIONS; B(C6F5)(3)-CATALYZED TRANSFER; ALPHA,BETA-UNSATURATED KETONES; CARBONYL-COMPOUNDS; N-ALKYLATION; PHARMACOLOGICAL-ACTIVITY; HANTZSCH ESTER; ALDEHYDES in [Zhan, Xiao-Yu; Zhang, Hua; Dong, Yu; Yang, Jian; Wang, Ji-Yu] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China; [Zhan, Xiao-Yu; Zhang, Hua; Dong, Yu; Yang, Jian] Univ Chinese Acad Sci, Beijing 100049, Peoples R China; [He, Shuai; Shi, Zhi-Chuan] Southwest Minzu Univ, Chengdu 610041, Peoples R China; [Tang, Lei] Sichuan Univ, West China Hosp, Translat Neurosci Ctr, Lab Anaesthesia & Crit Care Med, Chengdu 610041, Peoples R China; [Tang, Lei] Sichuan Univ, West China Hosp, Dept Anaesthesiol, Chengdu 610041, Peoples R China in 2020.0, Cited 109.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. HPLC of Formula: C15H12O
The B(C6F5)(3)-catalyzed chemoselective hydrosilylation of alpha,beta- and alpha,beta,gamma,delta-unsaturated ketones into the corresponding non-symmetric ketones in mild reaction conditions is developed. Nearly 55 substrates including those bearing reducible functional groups such as alkynyl, alkenyl, cyano, and aromatic heterocycles are chemoselectively hydrosilylated in good to excellent yields. Isotope-labeling studies revealed that hexafluoro-2-propanol also served as a hydrogen source in the process.
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Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com