30651-46-8

Upstream product

• 1093987-01-9 N-{2-[hydroxy(phenyl)methyl]phenyl}-L-prolinamide 
• 64-19-7 acetic acid 
• 13209-38-6 (2-aminophenyl)(phenyl)methanol 
• 108-24-7 acetic anhydride 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 85-99-4 2-acetamidobenzophenone 
• 28586-49-4 N-(2-(hydroxy(phenyl)methyl)phenyl)acetamide 

Downstream Products

• 30545-62-1 acetic acid (biphenyl-2-yl)(phenyl)methyl ester 

Relevant academic research and scientific papers

Sunlight-Driven Forging of Amide/Ester Bonds from Three Independent Components: An Approach to Carbamates

A photoredox catalytic route to carbamates enabled by visible irradiation (or simply sunlight) has been developed. This process leads to a novel approach to the construction of heterocyclic rings wherein the amide or ester motifs of carbamates were assembled from three isolated components. Large-scale experiments were realized by employing continuous flow techniques, and reuse of photocatalyst demonstrated the green and sustainable aspects of this method.

Enantiospecific synthesis of 5-phenylpyrrolo[2,1-c][1,4]benzodiazepines

Enantiomerically pure 5-phenylpyrrolo[2,1-c][1,4]benzodiazepines were synthesized starting from 2-aminobenzophenones and 2-amino-4-methoxyxanthone, using l-proline as a chiral building block.