An article Synergistic palladium/enamine catalysis for asymmetric hydrocarbon functionalization of unactivated alkenes with ketones WOS:000475661500013 published article about ALLYLIC ALKYLATION; TRANSITION-METAL; C-H; ALPHA-ALLYLATION; BOND ACTIVATION; ALDEHYDES; ORGANOCATALYSIS; AMINE; HYDROCARBOFUNCTIONALIZATION; COMPLEXES in [Wei, Chiyu; Ye, Xiaohan; Xing, Qingyu; Shi, Xiaodong] Univ S Florida, Dept Chem, Tampa, FL 33620 USA; [Xie, Yan] Quzhou Univ, Coll Chem & Mat Engn, Quzhou 324000, Peoples R China; [Hu, Yong] Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, Shanghai 200040, Peoples R China in 2019.0, Cited 43.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Category: benzodioxans
Synergistic palladium and enamine catalysis was explored to promote ketone addition to unactivated olefins. A secondary amine-based organocatalyst was identified as the optimal co-catalyst for the directed Pd-catalyzed alkene activation. Furthermore, asymmetric hydrocarbon functionalization of unactivated alkenes was also achieved with good to excellent yield (up to 96% yields) and stereoselectivity (up to 96% ee). This strategy presented an efficient approach to prepare alpha-branched ketone derivatives under mild conditions.
Category: benzodioxans. Welcome to talk about 100-19-6, If you have any questions, you can contact Wei, CY; Ye, XH; Xing, QY; Hu, Y; Xie, Y; Shi, XD or send Email.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem