Decrypt The Mystery Of 10466-61-2

《α-Chymotrypsin-catalyzed segment condensations via the kinetically controlled approach using carbamoylmethyl esters as acyl donors in organic media》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(H-Leu-NH2.HCl)Reference of H-Leu-NH2.HCl.

Reference of H-Leu-NH2.HCl. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: H-Leu-NH2.HCl, is researched, Molecular C6H15ClN2O, CAS is 10466-61-2, about α-Chymotrypsin-catalyzed segment condensations via the kinetically controlled approach using carbamoylmethyl esters as acyl donors in organic media. Author is Miyazawa, Toshifumi; Ensatsu, Eiichi; Hiramatsu, Makoto; Yanagihara, Ryoji; Yamada, Takashi.

The superiority of the carbamoylmethyl ester as an acyl donor for the α-chymotrypsin-catalyzed segment condensations via the kinetically controlled approach is demonstrated in several model systems carried out in organic media with low water content. Furthermore, this approach is successfully applied to the construction of the Leu-enkephalin sequence via a 4 + 1 segment coupling.

《α-Chymotrypsin-catalyzed segment condensations via the kinetically controlled approach using carbamoylmethyl esters as acyl donors in organic media》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(H-Leu-NH2.HCl)Reference of H-Leu-NH2.HCl.

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare