C. Oalmann

发表

Crystallographic structure of a small molecule SIRT1 activator-enzyme complex

F. Jiang, Beth L. Pietrak, T. Riera, 2014, Nature Communications.

Stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes as novel dipeptide isosteres

S. Martin, R. Austin, C. Oalmann, 1990 .

The Identification of the SIRT1 Activator SRT2104 as a Clinical Candidate

Amy V. Lynch, David P. Carney, P. J. Elliot, 2013 .

Enantioselective, rhodium catalyzed intramolecular cyclopropanations of homoallylic diazoacetates.

S. Liras, S. Martin, C. Oalmann, 1992 .

Enantioselective Intramolecular Cyclopropanations of Allylic and Homoallylic Diazoacetates and Diazoacetamides Using Chiral Dirhodium(II) Carboxamide Catalysts

S. Liras, M. Dwyer, M. Doyle, 1995 .

High enantioselectivity in the intramolecular cyclopropanation of allyl diazoacetates using a novel rhodium(II) catalyst

P. Mueller, R. Pieters, M. Doyle, 1991 .

Cyclopropanes as conformationally restricted peptide isosteres. Design and synthesis of novel collagenase inhibitors

S. Liras, S. Martin, C. Oalmann, 1993 .

1,2,3-trisubstituted cyclopropanes as conformationally restricted peptide isosteres: application to the design and synthesis of novel renin inhibitors.

S. Rosenberg, R. Austin, W. Baker, 1992, Journal of medicinal chemistry.