Orena's Team
Mario Orena
Professor of Organic Chemistry
Facoltá di Scienze
Universitá di Ancona
Tel : 39 71 220 4720
Fax : 39 71 220 4714
Silvano Geremia
Researcher of Inorganic Chemistry
Facoltá di Scienze
Universitá di Ancona
Tel : 39 71 220 4416
Roberta Galeazzi
Computational Chemistry Technician
Facoltá di Scienze
Universitá di Ancona
Tel : 39 71 220 4707
Giovanna Mobbili
PhD student
Universitá di Ancona
Tel : 39 71 220 4707
Fields of Interest:
- Enantioselective synthesis
- Chiral auxiliaries
- Synthesis of natural compounds with biological activity
- Enzymes in organic synthesis
- Organometallic chemistry
Selected references:
- Cardillo, G.; D'Amico, A.; Orena, M.; Sandri, S.
"Diastereoselective Alkylation of 3-Acylimidazolin-2-ones: Synthesis of
(R)- and (S)-Lavandulol" J. Org. Chem., 1988,
53, 2354-2356.
- Cardillo, G.; Orena, M.; Romero, M.; Sandri, S. "Enantioselective
Synthesis of 2-Benzyloxyalcohols and 1,2-Diols via Alkylation of Chiral
Glycolate Imides. A Convenient Approach to Optically Active Glycerol
Derivatives" Tetrahedron, 1989, 45, 1501-1508.
- Bongini, A.; Cardillo, G.; Orena, M.; Sabatino, P.; Sandri, S. "New
Synthesis of 4,5-Dihydro-1,3-oxazoles and 4,5-Dihydro-1,3-oxazines, Useful
Intermediates to Enantiomerically Pure Aminodiols" J. Chem. Soc., Perkin
Trans. I, 1990, 3095-3101.
- Orena, M.; Porzi, G.; Sandri, S. "A New Approach to 2-Phenylthioalcohols
in High Optical Purity" Tetrahedron Lett., 1992, 33,
3797-3800;
- Orena. M.; Porzi, G.; Sandri, S. "A New Synthesis of Both Enantiomers of
endo-Norborn-5-en-2-ylmethanol" J. Chem. Res., (S), 1992,
42-43.
- Mobbili, G.; Orena, M.; Porzi, G.; Sandri, S. "Synthesis of
(+)-Eldanolide, the Sex Pheromone of Eldana saccharina, by
Enantioselective Alkylation of a Chiral Imide" J. Chem. Res., (S),
1993, 230-231.
- Cardillo, B.; Galeazzi, R.; Mobbili, G.; Orena, M.; Rossetti, M.,
"Diastereoselective Hetero-Diels-Alder Cycloaddition of a C-Nitroso Compound
Prepared Starting from a Homochiral Imidazolidin-2-one" Tetrahedron:
Asymmetry, 1994, 5, 1535-1540.
- Cardillo, G.; Orena, M.; Sandri, S.; Tomasini, C., "An Efficient
Synthesis of (R)-(+)- and (S)-(-)-Propranolol from Resolved
5-Iodomethyloxazolidin-2-ones" Tetrahedron, 1987, 43,
2505-2512
- Bongini, A.; Cardillo, G.; Orena, M.; Porzi, G.; Sandri, S.; "A New
Synthesis of Both the Enantiomers of 4-Amino-3-hydroxybutanoic Acid (GABOB) and
MM2 Calculations for Rotamers of the Intermediate Oxazolidin-2-ones"
Tetrahedron, 1987, 43, 4377-4383.
- Bongini, A.; Cardillo, G.; Orena, M.; Porzi, G.; Sandri, S., "Synthesis
of Aminoalcohols via Perihydro-1,3-oxazin-2-ones and Absolute
Configuration Assignment through MM2 Calculation" Chem. Lett.,
1988, 87-90.
- Bruni, E.; Cardillo, G.; Orena, M.; Sandri, S.; Tomasini, C., "Synthesis
of Chiral 1,2-Diamines" Tetrahedron Lett., 1989, 30,
1679-1682.
- Orena, M.; Porzi, G.; Sandri, S., "A New Synthesis of (R)-GABOB
and (R)-Oxiracetam" J. Chem. Res., (S), 1990, 376;
(M), 1990, 2701-2711
- Cardillo, G.; Orena, M.; Penna, M.; Sandri, S.; Tomasini, C., "Synthesis
of (R)-N-Tosylemeriamine via Chiral N-Tosylimidazolidin-2-ones"
Synlett, 1990, 543-544
- Cardillo, G.; Orena, M.; Penna, M.; Sandri, S.; Tomasini, "A New
Approach to the Synthesis of Enantiomerically Pure 2,3-Diaminoacids through
Chiral Imidazolidin-2-ones" C., Tetrahedron, 1991, 47,
2263-2272
- Orena, M.; Porzi, G.; Sandri, S., "Diastereoselective Alkylation of
(3S)- and (3R)-Methylpiperazin-2,5-dione Derivatives. A
Convenient Approach to Both (S)- and (R)-Alanine" J. Org.
Chem., 1992, 57, 6532-6536
- Orena, M.; Porzi, G.; Sandri, S., "(3R)- and
(3S)-Methylpiperazine-2,5-dione Derivatives as Useful Intermediates in
the Enantioselective Synthesis of [[alpha]]-Amino Esters" J. Chem. Res.,
(S), 1993, 318-319; (M), 1993, 2125-2152
- Cardillo, B.; Galeazzi, R.; Mobbili, G.; Orena, M.; Rossetti, M.,
"Synthesis and Structural Assignment of Diastereomerically Pure N-Substituted
4-Alkylpyrrolidin-2-ones, Intermediates for the Preparation of
3-Alkylpyrrolidines in Both Enantiomerically Pure Forms" Heterocycles,
1994, 38, 2663-2676.