Sreenivasa R. Mundla
Eli Lilly (United States)(US)Albany Molecular Research (United States)(US)
Publications by Year
Research Areas
Chemical Reaction Mechanisms, Synthesis and Characterization of Heterocyclic Compounds, TGF-β signaling in diseases, Microbial Applications in Construction Materials, Quinazolinone synthesis and applications
Most-Cited Works
- → Optimization of a Dihydropyrrolopyrazole Series of Transforming Growth Factor-β Type I Receptor Kinase Domain Inhibitors: Discovery of an Orally Bioavailable Transforming Growth Factor-β Receptor Type I Inhibitor as Antitumor Agent(2008)66 cited
- → Dihydropyrrolopyrazole Transforming Growth Factor-β Type I Receptor Kinase Domain Inhibitors: A Novel Benzimidazole Series with Selectivity versus Transforming Growth Factor-β Type II Receptor Kinase and Mixed Lineage Kinase-7(2006)48 cited
- → A novel method for the efficient synthesis of 2-arylamino-2-imidazolines(2000)26 cited
- → A concise synthesis of quinazolinone TGF-β RI inhibitor through one-pot three-component Suzuki–Miyaura/etherification and imidate–amide rearrangement reactions(2007)17 cited
- → Regioselective synthesis of 4-halo ortho-dinitrobenzene derivatives(2000)15 cited
- → Studies on the Rh and Ir mediated tandem Pauson–Khand reaction. A new entry into the dicyclopenta[a,d]cyclooctene ring system(2003)12 cited
- → A new method for the synthesis of 2,6-dinitro and 2-halo-6-nitrostyrenes(2000)5 cited
- → ChemInform Abstract: A Concise Synthesis of Quinazolinone TGF‐β RI Inhibitor Through One‐Pot Three‐Component Suzuki—Miyaura/Etherification and Imidate—Amide Rearrangement Reactions.(2008)
- → ChemInform Abstract: Regioselective Synthesis of 4‐Halo ortho‐Dinitrobenzene Derivatives.(2000)
- → ChemInform Abstract: A Novel Method for the Efficient Synthesis of 2‐Arylamino‐2‐imidazolines.(2000)