In 2020.0 J AM CHEM SOC published article about CROSS-COUPLING REACTIONS; UNACTIVATED ALKENES; AMINO-ACIDS; HYDROCARBOFUNCTIONALIZATION; PHOSPHONATES; PALLADIUM; ARYLATION; REAGENTS; LIGANDS in [He, Shi-Jiang; Wang, Jia-Wang; Li, Yan; Xu, Zhe-Yuan; Wang, Xiao-Xu; Lu, Xi; Fu, Yao] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Urban Pollutant Convers, iChEM,Anhui Prov Key Lab Biomass Clean Energy, Hefei 230026, Peoples R China in 2020.0, Cited 68.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. COA of Formula: C7H8O
Substantial advances in enantioconvergent C(sp(3))-C(sp(3)) bond formation reactions have been made in recent years through the use of transition-metal-catalyzed cross-coupling reactions of racemic secondary alkyl electrophiles with organometallic reagents. Herein, we report a general process for the asymmetric construction of alkyl-alkyl bonds adjacent to heteroatoms, namely, a nickel-catalyzed enantioconvergent reductive hydroalkylation of olefins with alpha-heteroatom phosphorus or sulfur alkyl electrophiles. Including the use of readily available olefins, this reaction has considerable advantages, such as mild reaction conditions, a broad substrate scope, and good functional group compatibility, making it a desirable alternative to traditional electrophile-nucleophile cross-coupling reactions.
COA of Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact He, SJ; Wang, JW; Li, Y; Xu, ZY; Wang, XX; Lu, X; Fu, Y or concate me.
Reference:
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