Maurizio Franzini
Affiliations: | 2000-2005 | Chemistry | Stanford University, Palo Alto, CA |
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"Maurizio Franzini"Mean distance: 7.64 | S | N | B | C | P |
Parents
Sign in to add mentor| Barry M. Trost | grad student | 2000-2005 | Stanford | |
| (Molybdenum and palladium catalyzed asymmetric allylic alkylation of prochiral nucleophiles: Enantioselective synthesis of nonnatural alpha-amino acids and of tertiary alpha-hydroxy carboxylic acid derivatives.) | ||||
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| Franzini M, Ye XM, Adler M, et al. (2013) Triazolopyridazine LRRK2 kinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 1967-73 |
| Garofalo AW, Adler M, Aubele DL, et al. (2013) Discovery of 4-alkylamino-7-aryl-3-cyanoquinoline LRRK2 kinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 1974-7 |
| Garofalo AW, Adler M, Aubele DL, et al. (2013) Novel cinnoline-based inhibitors of LRRK2 kinase activity. Bioorganic & Medicinal Chemistry Letters. 23: 71-4 |
| Tsuhako AL, Brown DS, Koltun ES, et al. (2012) The design, synthesis, and biological evaluation of PIM kinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 22: 3732-8 |
| Rice KD, Kim MH, Bussenius J, et al. (2012) Pyrazolopyrimidines as dual Akt/p70S6K inhibitors. Bioorganic & Medicinal Chemistry Letters. 22: 2693-7 |
| Trost BM, Dogra K, Franzini M. (2004) 5H-oxazol-4-ones as building blocks for asymmetric synthesis of alpha-hydroxycarboxylic acid derivatives. Journal of the American Chemical Society. 126: 1944-5 |
| Zanoni G, Porta A, Meriggi A, et al. (2002) 1,2-Oxopalladation versus pi-allyl palladium route. A regioconvergent approach to a key intermediate for cyclopentanoids synthesis. New insights into the Pd(II)-catalyzed lactonization reaction. The Journal of Organic Chemistry. 67: 6064-9 |