137569-76-7

Upstream product

• 885956-81-0 ethyl 1-benzyl-4-phenyl-2,5-dihydro-1H-pyrrole-3-carboxylate 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 137569-75-6 1H-pyrrole-3-carboxylic acid, 2,5-dihydro-1-methyl-4-phenyl-, ethyl ester 
• 50893-53-3 carbonochloridic acid 1-chloro-ethyl ester 

Downstream Products

• 137569-69-8 1H-pyrrole-3-carboxylic acid, 2,5-dihydro-4-phenyl-, monohydrochloride 

Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6

The present disclosure relates to compounds capable of modulating the activity of NR2F6. The compounds of the disclosure may be used in methods for the prevention and/or the treatment of diseases and disorders associated with modulating NR2F6 activity.

Process for the preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carbocyclic acids

The present invention relates to a process for the preparation of cis substituted cyclic β-aryl or heteroaryl carboxylic acid derivatives in high diastereo- and enantioselectivity by enantioselective hydrogenation in accordance with the following scheme w

β-Proline Analogues as Agonists at the Strychnine-Sensitive Glycine Receptor

3-Carboxy-3,4-dehydropyrrolidine was found to bind with affinity equal to that of glycine in a strychnine binding assay.Simple substitution of the 1-, 2-, 4-, or 5-position resulted in marked loss of affinity.A decaline in affinity was also found upon