Michael J. Alberti
Triangle(US)High Throughput Biology (United States)(US)
Publications by Year
Research Areas
Synthesis and biological activity, Melanoma and MAPK Pathways, Quinazolinone synthesis and applications, Carbohydrate Chemistry and Synthesis, Synthetic Organic Chemistry Methods
Most-Cited Works
- → Pyrazolo[1,5-a]pyridines as p38 Kinase Inhibitors(2005)87 cited
- → Tandem Glycolate Claisen Rearrangement/Ring-Closing Metathesis: A Stereochemically General Synthesis of Substituted Dihydropyran-2-carboxylates(1998)45 cited
- → The identification of pyrazolo[1,5-a]pyridines as potent p38 kinase inhibitors(2008)43 cited
- → (1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors(2005)43 cited
- → Discovery and in vitro evaluation of potent kinase inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4-d]pyrimidines(2005)34 cited
- → Corrigendum to “(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors” [Bioorg. Med. Chem. Lett. 15 (2005) 3402–3406](2015)1 cited
- → ChemInform Abstract: Tandem Glycolate Claisen Rearrangement/Ring‐Closing Metathesis: Stereochemically General Synthesis of Substituted Dihydropyran‐2‐carboxylates.(1998)1 cited
- → Discovery and in vitro Evaluation of Potent Kinase Inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4‐d]pyrimidines.(2006)1 cited