859963-94-3

Upstream product

• 62-53-3 aniline 
• 102-04-5 1,3-Diphenylpropanone 
• 122-78-1 phenylacetaldehyde 
• 100-39-0 benzyl bromide 
• 6921-34-2 benzylmagnesium chloride 
• 118-92-3 anthranilic acid 
• 857580-90-6 N-(1-benzyl-2-phenyl-ethyl)-anthranilic acid-(4-chloro-anilide) 
• 24122-31-4 3-(4-chlorophenyl)quinazolin-4(3H)-one 
• 16347-60-7 3-phenyl-4(3H)-quinazolinone 
• 857589-17-4 N-(1-benzyl-2-phenyl-ethyl)-anthranilic acid 
• 857580-91-7 N-(1-benzyl-2-phenyl-ethyl)-anthranilic acid anilide 

Relevant academic research and scientific papers

Palladium-Catalyzed Enantioselective C-H Aminocarbonylation: Synthesis of Chiral Isoquinolinones

A Pd-catalyzed enantioselective C-H carbonylation by desymmetrization was developed with commercially available L-pyroglutamic acid as chiral ligand. Isoquinolinones were successfully obtained with good yields and high enantioselectivities. Mechanistic studies and DFT calculations provided a reasonable reaction pathway.

Efficient three-component one-pot benzylation and allylation of aldehydes and amines for synthesis of homobenzylamines and homoallylamines

(Chemical Equation Presented) A highly efficient, three-component one-pot benzylation and allylation of aromatic and aliphatic aldehydes and amines affords the corresponding homobenzylamines and homoallylamines in good to excellent yield. The procedure is