1399210-35-5

Upstream product

• 1399209-89-2 C₃₆H₂₉N₃O₄ 
• 1399210-33-3 C₂₄H₂₄N₂O₄ 
• 71112-99-7 N’-(2-methoxyphenylmethylene)benzohydrazide 
• 91098-98-5 N’-benzoyl-2-methoxybenzohydrazine 
• 135-02-4 ortho-anisaldehyde 
• 24461-61-8 phenylglycine methyl ester 
• 83572-73-0 methyl (E)-2-((2-methoxybenzylidene)amino)-2-phenylacetate 

Relevant academic research and scientific papers

Rh-catalyzed asymmetric hydrogenation of racemic aldimines via dynamic kinetic resolution

Catalyzed by a rhodium complex of P-stereogenic diphosphine ligand trichickenfootphos (TCFP), asymmetric hydrogenation of racemic aldimines via dynamic kinetic resolution has been realized for the preparation of chiral arylglycines with good yields and enantioselectivities.

A catalytic asymmetric Ugi-type reaction with acyclic azomethine imines

An unconventional Ugi: A catalytic asymmetric Ugi-type reaction can be realized by use of N'-alkylbenzohydrazide, instead of a conventional amine, in the presence of an axially chiral dicarboxylic acid. The reaction proceeds through a key acyclic azomethi