An article Highly enantioselective carbene insertion into N-H bonds of aliphatic amines WOS:000498849000040 published article about THERMOCHEMICAL KINETICS; EQUILIBRIUM ACIDITIES; DENSITY FUNCTIONALS; CONJUGATE ADDITION; MICHAEL ADDITION; DIAZO-COMPOUNDS; BASIS-SETS; CATALYSIS; CARBON; ORGANOCATALYSTS in [Zhu, Shou-Fei; Zhou, Qi-Lin] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China; Nankai Univ, Coll Chem, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China in 2019, Cited 67. Safety of Diphenylmethanamine. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9
Aliphatic amines strongly coordinate, and therefore easily inhibit, the activity of transition-metal catalysts, posing a marked challenge to nitrogen-hydrogen (N-H) insertion reactions. Here, we report highly enantioselective carbene insertion into N-H bonds of aliphatic amines using two catalysts in tandem: an achiral copper complex and chiral amino-thiourea. Coordination by a homoscorpionate ligand protects the copper center that activates the carbene precursor. The chiral amino-thiourea catalyst then promotes enantioselective proton transfer to generate the stereocenter of the insertion product. This reaction couples a wide variety of diazo esters and amines to produce chiral alpha-alkyl alpha-amino acid derivatives.
Welcome to talk about 91-00-9, If you have any questions, you can contact Li, ML; Yu, JH; Li, YH; Zhu, SF; Zhou, QL or send Email.. Safety of Diphenylmethanamine
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Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics