An article Nickel-Catalyzed Asymmetric Reductive 1,2-Carboamination of Unactivated Alkenes WOS:000504477000001 published article about CARBOAMINATION REACTIONS; ELECTROPHILIC AMINATION; INTRAMOLECULAR CARBOAMINATION; STEREOCONTROLLED SYNTHESIS; BOND FORMATION; OLEFINS; DICARBOFUNCTIONALIZATION; CYCLIZATION; FUNCTIONALIZATION; HYDROAMINATION in [He, Jun; Xue, Yuhang; Han, Bo; Zhang, Chunzhu; Wang, You; Zhu, Shaolin] Nanjing Univ, Sch Chem & Chem Engn, Chem & Biomed Innovat Ctr ChemBIC, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China in 2020.0, Cited 99.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Safety of m-Methoxyphenol
Starting from diverse alkene-tethered aryl iodides and O-benzoyl-hydroxylamines, the enantioselective reductive cross-electrophilic 1,2-carboamination of unactivated alkenes was achieved using a chiral pyrox/nickel complex as the catalyst. This mild, modular, and practical protocol provides rapid access to a variety of beta-chiral amines with an enantioenriched aryl-substituted quaternary carbon center in good yields and with excellent enantioselectivities. This process reveals a complementary regioselectivity when compared to Pd and Cu catalysis.
Safety of m-Methoxyphenol. Welcome to talk about 150-19-6, If you have any questions, you can contact He, J; Xue, YH; Han, B; Zhang, CZ; Wang, Y; Zhu, SL or send Email.
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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