Hydrolysis of an amide in a carboxypeptidase model using cobalt (III) and bifunctional catalysts

A Schepartz, R Breslow

Index: Journal of the American Chemical Society, , vol. 109, # 6 p. 1814 - 1826

Full Text: HTML

Citation Number: 88

Abstract

... It seemed to us that a study of a complete model for carbox- ypeptidase might help to elucidate several questions ... Chemical Society: Washington, DC, 1971; Chapter 2. (1 1) Cotton, F. A,; Wilkinson, G. Advanced Inorganic Chemistry, 4th ed ... 0 1987 American Chemical Society ...

Related Articles:

Preparation of novel antibacterial agents. Replacement of the central aromatic ring with heterocycles

[Li, Jianke; Wakefield, Brian D.; Ruble, J. Craig; Stiff, Cory M.; Romero, Donna L.; Marotti, Keith R.; Sweeney, Michael T.; Zurenko, Gary E.; Rohrer, Douglas C.; Thorarensen, Atli Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 8 p. 2347 - 2350]

Effect of terminal group sterics and dendron packing on chirality transfer from the central core of a dendrimer

[Gandhi, Preete; Huang, Baohua; Gallucci, Judith C.; Parquette, Jon R. Organic Letters, 2001 , vol. 3, # 20 p. 3129 - 3132]

Selective urokinase-type plasminogen activator inhibitors. 4. 1-(7-sulfonamidoisoquinolinyl) guanidines

[Journal of Medicinal Chemistry, , vol. 50, # 10 p. 2341 - 2351]

A high yielding synthesis of anthranilate esters from sterically hindered alcohols

[Tetrahedron Letters, , vol. 42, # 9 p. 1785 - 1788]

Synthesis of simple analogues of methyllycaconitine—an efficient method for the preparation of the N-substituted anthranilate pharmacophore

[Tetrahedron, , vol. 60, # 28 p. 5953 - 5963]

More Articles...