Gilbert O. Chandler
Merck & Co., Inc., Rahway, NJ, USA (United States)(US)
Publications by Year
Research Areas
Synthesis of β-Lactam Compounds, Protease and Inhibitor Mechanisms, Metal complexes synthesis and properties, Cell Adhesion Molecules Research, Chemical Synthesis and Analysis
Most-Cited Works
- → Cephalosporin antibiotics can be modified to inhibit human leukocyte elastase(1986)166 cited
- → Orally Active .beta.-Lactam Inhibitors of Human Leukocyte Elastase. 3. Stereospecific Synthesis and Structure-Activity Relationships for 3,3-Dialkylazetidin-2-ones(1995)89 cited
- → Inhibition of human leukocyte elastase. 1. Inhibition by C-7-substituted cephalosporin tert-butyl esters(1990)73 cited
- → Orally active .beta.-lactam inhibitors of human leukocyte elastase-1. Activity of 3,3-diethyl-2-azetidinones(1992)68 cited
- → Inhibition of human leukocyte elastase. 4. Selection of a substituted cephalosporin (L-658,758) as a topical aerosol(1992)53 cited
- → Inhibition of human leukocyte elastase. 3. Synthesis and activity of 3'-substituted cephalosporins(1990)48 cited
- → Chemical, biochemical, pharmacokinetic, and biological properties of L-680,833: a potent, orally active monocyclic beta-lactam inhibitor of human polymorphonuclear leukocyte elastase.(1993)34 cited
- → Monocyclic β-lactam inhibitors of human leukocyte elastase. Stereospecific synthesis and activity of 3,4-disubstituted-2-azetidinones.(1993)14 cited
- → ChemInform Abstract: Orally Active β‐Lactam Inhibitors of Human Leukocyte Elastase. Part 3. Stereospecific Synthesis and Structure‐Activity Relationships for 3,3‐Dialkylazetidin‐2‐ones.(1995)5 cited
- → ChemInform Abstract: Inhibition of Human Leukocyte Elastase. Part 3. Synthesis and Activity of 3′‐Substituted Cephalosporins.(1991)3 cited