102284-29-7

Upstream product

• 15761-39-4 N-Boc-L-proline 
• 95-55-6 2-amino-phenol 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 

Downstream Products

• 102284-34-4 2-(N-boc-L-prolinamido)phenyl N-phenylcarbamate 
• 102284-39-9 2-(L-prolinamido)phenyl N-phenylcarbamate hydrochloride 
• 92279-30-6 2-<(methoxysuccinyl)-L-alanyl-L-alanyl-L-prolinamido>phenyl N-phenylcarbamate 

Relevant academic research and scientific papers

Direct asymmetric aldol reaction catalyzed by simple prolinamide phenols

Simple prolinamides 1a-f were synthesized, and their catalytic effects on the direct asymmetric aldol reactions in organic solvents and in water were evaluated. Prolinamide phenols 1a-d were found to be effective catalysts for the reaction of aromatic ald

Prolinamides derived from aminophenols as organocatalysts for asymmetric direct aldol reactions

N-(2-Hydroxyphenyl)-prolinamides were synthesized with the aim to introduce an additional hydrogen bonding site to the prolinamide structure. These compounds were evaluated as organocatalysts for asymmetric aldol reactions between aromatic aldehydes and c

Peptidyl Carbamates Incorporating Amino Acid Isosteres as Novel Elastase Inhibitors

The design and synthesis of 13 novel peptidyl carbamates are described.When tested for inhibitory activity toward porcine pancreatic elastase, trypsin, and chymotrypsin, six compounds were found to specifically inhibit lastase without affecting the other