Robert M. Rzasa
Publications by Year
Research Areas
Synthetic Organic Chemistry Methods, Synthesis and Catalytic Reactions, Molecular spectroscopy and chirality, Asymmetric Synthesis and Catalysis, Catalytic C–H Functionalization Methods
Most-Cited Works
- → Total Synthesis and Immunosuppressive Activity of (−)-Pateamine A and Related Compounds: Implementation of a β-Lactam-Based Macrocyclization(1998)149 cited
- → Novel Vanilloid Receptor-1 Antagonists: 2. Structure−Activity Relationships of 4-Oxopyrimidines Leading to the Selection of a Clinical Candidate(2007)98 cited
- → Discovery and in Vivo Evaluation of (S)-N-(1-(7-Fluoro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)-9H-purin-6-amine (AMG319) and Related PI3Kδ Inhibitors for Inflammation and Autoimmune Disease(2014)85 cited
- → Palladium-Catalyzed Chemoselective Monoarylation of Hydrazides for the Synthesis of [1,2,4]Triazolo[4,3-a]pyridines(2010)78 cited
- → Total Synthesis of the Novel, Immunosuppressive Agent (−)-Pateamine A from Mycale sp. Employing a β-Lactam-Based Macrocyclization(1998)70 cited
- → Discovery of Highly Selective and Potent p38 Inhibitors Based on a Phthalazine Scaffold(2008)58 cited
- → Novel Vanilloid Receptor-1 Antagonists: 1. Conformationally Restricted Analogues oftrans-Cinnamides(2007)42 cited
- → Structure–activity relationships of 3,4-dihydro-1H-quinazolin-2-one derivatives as potential CDK5 inhibitors(2007)37 cited
- → Isolation and Identification of Eukaryotic Initiation Factor 4A as a Molecular Target for the Marine Natural Product Pateamine A(2007)31 cited
- → Design and synthesis of quinolin-2(1H)-one derivatives as potent CDK5 inhibitors(2007)27 cited