Flavia Messina
University College Dublin(IE)
Publications by Year
Research Areas
Asymmetric Synthesis and Catalysis, Catalytic C–H Functionalization Methods, Synthesis and Catalytic Reactions, Carbohydrate Chemistry and Synthesis, Asymmetric Hydrogenation and Catalysis
Most-Cited Works
- → Chiral Azole Derivatives. 4.1 Enantiomers of Bifonazole and Related Antifungal Agents: Synthesis, Configuration Assignment, and Biological Evaluation(2000)57 cited
- → Resolution of (±)-1-Aryl-2-propynylamines via Acyltransfer Catalyzed byCandida antarcticaLipase(1999)52 cited
- → A new stereoselective synthesis of chiral γ-functionalized (E)-allylic amines(1996)51 cited
- → Chiral azole derivatives. Part 5: Synthesis of enantiomerically pure 1-[α-(benzofuran-2-yl)arylmethyl]-1H-1,2,4-triazoles, antifungal and antiaromatase agents(2000)24 cited
- → Solid phase synthesis of 2,6-disubstituted-4(3H)-pyrimidinones targeting HIV-1 reverse transcriptase(1998)17 cited
- → Stereoselective synthesis of α-aryl-2-benzofuranmethanamines and α-aryl-1H-indole-2-methanamines through palladium-mediated annulation of chiral α-arylpropargylamines(2000)17 cited
- → Chiral azole derivatives, 3. Synthesis of the enantiomers of the potent aromatase inhibitor 1-[2-benzofuranyl(4-chlorophenyl)methyl]-1H-imidazole(1999)15 cited
- → Cyclopenta[d]pyrimidines and Dihydropyrrolo[2,3‐d]pyrimidines as Potent and Selective Corticotropin‐Releasing Factor 1 Receptor Antagonists(2007)14 cited
- → Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety(2005)11 cited
- → Palladium-catalysed reduction of 3-substituted cephems. A high yield approach to ceftizoxime synthetic intermediates(1997)6 cited