Now Is The Time For You To Know The Truth About 56-85-9

Future efforts will undeniably focus on the diversification of the new catalytic transformations. These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. Keep reading other articles of 56-85-9. Product Details of 56-85-9.

Having gained chemical understanding at molecular level, chemistry graduates may choose to apply this knowledge in almost unlimited ways, as it can be used to analyze all matter and therefore our entire environment. 56-85-9, Name is H-Gln-OH, molecular formula is , belongs to pyrrolines compound. In a document, author is Nagao, Y, Product Details of 56-85-9.

Synthesis of a new class of cathepsin B inhibitors exploiting a unique reaction cascade

Chiral 5-substituted 3-pyrrolin-2-ones bearing L-Ile-L-Pro-OH or L-Phe-NHCH2Ph were successfully synthesized by utilizing a characteristic reaction cascade based on alkaline hydrolysis of the corresponding diethyl alpha-hydroxy-alpha-(beta-propiolamide)malonates. Among the synthesized chiral pyrrolinones, compound 5S-9 proved to be the most potent inhibitor against cathepsin B, (C) 2000 Elsevier Science Ltd. All rights reserved.

Future efforts will undeniably focus on the diversification of the new catalytic transformations. These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. Keep reading other articles of 56-85-9. Product Details of 56-85-9.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem