Comparison of deacylation rates of chymotryptic catalysis within an enantiomeric pair of p-nitrophenyl esters

谷沢和隆， 山田浩之， 伊藤邦彦， 金岡祐一

Index: Chemical and Pharmaceutical Bulletin, , vol. 39, # 10 p. 2748 - 2749

Full Text: HTML

Citation Number: 0

Abstract

Page 1. Pharmaceutical Society of Japan NII-Electronic Library Service PharmaceuticalSociety of Japan 2748 Notes Chem, Pharm. BuU. 39(10) 2748-2749 (1991) Vel,39,No. 10 Comparison ef Deacylation Rates of Chymotryptic Catalysiswithin an p-Nitrophenyl Esters ...

Related Articles:

Kinetic Resolution of α??Substituted Alkanoic Acids Promoted by Homobenzotetramisole

[Chemistry - A European Journal, , vol. 17, # 40 p. 11296 - 11304]

Promotion of multipoint covalent immobilization through different regions of genetically modified penicillin G acylase from E. coli

[Process Biochemistry, , vol. 45, # 3 p. 390 - 398]

Dynamic enzymatic resolution of thioesters

[Journal of the American Chemical Society, , vol. 120, # 23 p. 5605 - 5610]

A stereoselective approach for the total synthesis of [2 (S)-phenyl-propionyl]-2-piperidinone-3-(R)-yl-ester and its diastereomer

[Tetrahedron, , vol. 69, # 10 p. 2319 - 2326]

A stereoselective approach for the total synthesis of [2 (S)-phenyl-propionyl]-2-piperidinone-3-(R)-yl-ester and its diastereomer

[Tetrahedron, , vol. 69, # 10 p. 2319 - 2326]

More Articles...