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1. Grisenti, P; Magni, A; Olgiati, V; Manzocchi, A; Ferraboschi, P; Villani, V; Pucciariello, R; Celotti, F
   Substrate interaction with 5 alpha-reductase enzyme: influence of the 17 beta-chain chirality in the mechanism of action of 4-azasteroid inhibitors
   STEROIDS
   
   P. Grisenti et al., "Substrate interaction with 5 alpha-reductase enzyme: influence of the 17 beta-chain chirality in the mechanism of action of 4-azasteroid inhibitors", STEROIDS, 66(11), 2001, pp. 803-810
2. CONCAS A; MOSTALLINO MC; PORCU P; FOLLESA P; BARBACCIA ML; TRABUCCHI M; PURDY RH; GRISENTI P; BIGGIO G
   ROLE OF BRAIN ALLOPREGNANOLONE IN THE PLASTICITY OF GAMMA-AMINOBUTYRIC-ACID TYPE-A RECEPTOR IN RAT-BRAIN DURING PREGNANCY AND AFTER DELIVERY
   Proceedings of the National Academy of Sciences of the United Statesof America
   
   A. Concas et al., "ROLE OF BRAIN ALLOPREGNANOLONE IN THE PLASTICITY OF GAMMA-AMINOBUTYRIC-ACID TYPE-A RECEPTOR IN RAT-BRAIN DURING PREGNANCY AND AFTER DELIVERY", Proceedings of the National Academy of Sciences of the United Statesof America, 95(22), 1998, pp. 13284-13289
3. GRISENTI P; MAGNI A; MANZOCCHI A; FERRABOSCHI P
   A PRACTICAL ROUTE FOR THE SYNTHESIS OF 17-SUBSTITUTED-STEROIDAL-3-THIOXAMIDES
   Steroids
   
   P. Grisenti et al., "A PRACTICAL ROUTE FOR THE SYNTHESIS OF 17-SUBSTITUTED-STEROIDAL-3-THIOXAMIDES", Steroids, 62(6), 1997, pp. 504-506
4. FERRABOSCHI P; GRISENTI P; SANTANIELLO E
   SYNTHESIS OF ONE DIASTEREOMERIC COUPLE OF THE MUCOLYTIC DRUG DOMIODOL,2R,S)-2-IODOMETHYL-4-HYDROXYMETHYL-1,3-DIOXOLANE] FROM D-MANNITOL ASCHIRAL STARTING MATERIAL
   Chirality
   
   P. Ferraboschi et al., "SYNTHESIS OF ONE DIASTEREOMERIC COUPLE OF THE MUCOLYTIC DRUG DOMIODOL,2R,S)-2-IODOMETHYL-4-HYDROXYMETHYL-1,3-DIOXOLANE] FROM D-MANNITOL ASCHIRAL STARTING MATERIAL", Chirality, 7(8), 1995, pp. 623-625
5. FERRABOSCHI P; GRISENTI P; MANZOCCHI A; SANTANIELLO E
   REGIOSELECTIVITY AND ENANTIOSELECTIVITY OF PSEUDOMONAS-CEPACIA LIPASEIN THE TRANSESTERIFICATION OF 2-SUBSTITUTED-1,4-BUTANEDIOLS
   Tetrahedron : asymmetry
   
   P. Ferraboschi et al., "REGIOSELECTIVITY AND ENANTIOSELECTIVITY OF PSEUDOMONAS-CEPACIA LIPASEIN THE TRANSESTERIFICATION OF 2-SUBSTITUTED-1,4-BUTANEDIOLS", Tetrahedron : asymmetry, 5(4), 1994, pp. 691-698
6. FERRABOSCHI P; CASATI S; GRISENTI P; SANTANIELLO E
   ENANTIOSELECTIVE PSEUDOMONAS-FLUORESCENS (P-CEPACIA) LIPASE-CATALYZEDIRREVERSIBLE TRANSESTERIFICATION OF 2-METHYL-1,2-DIOLS IN AN ORGANIC-SOLVENT
   Tetrahedron : asymmetry
   
   P. Ferraboschi et al., "ENANTIOSELECTIVE PSEUDOMONAS-FLUORESCENS (P-CEPACIA) LIPASE-CATALYZEDIRREVERSIBLE TRANSESTERIFICATION OF 2-METHYL-1,2-DIOLS IN AN ORGANIC-SOLVENT", Tetrahedron : asymmetry, 5(10), 1994, pp. 1921-1924
7. FERRABOSCHI P; CASATI S; GRISENTI P; SANTANIELLO E
   ENANTIOSELECTIVE PSEUDOMONAS-FLUORESCENS (P-CEPACIA) LIPASE-CATALYZEDIRREVERSIBLE TRANSESTERIFICATION OF 2-METHYL-1,2-DIOLS IN AN ORGANIC-SOLVENT
   Tetrahedron : asymmetry
   
   P. Ferraboschi et al., "ENANTIOSELECTIVE PSEUDOMONAS-FLUORESCENS (P-CEPACIA) LIPASE-CATALYZEDIRREVERSIBLE TRANSESTERIFICATION OF 2-METHYL-1,2-DIOLS IN AN ORGANIC-SOLVENT", Tetrahedron : asymmetry, 5(10), 1994, pp. 1921-1924
8. FERRABOSCHI P; GRISENTI P; CASATI S; SANTANIELLO E
   A NEW SYNTHESIS OF (R)-MEVALONOLACTONE AND (S)-MEVALONOLACTONE FROM THE ENZYMATIC RESOLUTION OF (R,S)-2-(3-METHYL-2-BUTENYL)-OXIRANEMETHANOL
   Synlett
   
   P. Ferraboschi et al., "A NEW SYNTHESIS OF (R)-MEVALONOLACTONE AND (S)-MEVALONOLACTONE FROM THE ENZYMATIC RESOLUTION OF (R,S)-2-(3-METHYL-2-BUTENYL)-OXIRANEMETHANOL", Synlett, (9), 1994, pp. 754-756
9. FERRABOSCHI P; CASATI S; DEGRANDI S; GRISENTI P; SANTANIELLO E
   AN INSIGHT INTO THE ACTIVE-SITE OF PSEUDOMONAS-FLUORESCENS (P-CEPACIA) LIPASE TO DEFINE THE STEREOCHEMICAL DEMAND FOR THE TRANSESTERIFICATION IN ORGANIC-SOLVENTS
   Biocatalysis
   
   P. Ferraboschi et al., "AN INSIGHT INTO THE ACTIVE-SITE OF PSEUDOMONAS-FLUORESCENS (P-CEPACIA) LIPASE TO DEFINE THE STEREOCHEMICAL DEMAND FOR THE TRANSESTERIFICATION IN ORGANIC-SOLVENTS", Biocatalysis, 10(1-4), 1994, pp. 279-288
10. FERRABOSCHI P; GRISENTI P; SANTANIELLO E
    A FACILE SYNTHESIS OF PENTADEUTERATED DOMIODOL (2-IODOMETHYL-4-HYDROXYMETHYL-1,3-DIOXOLANE) FROM GLYCEROL-1,1,2,3,3-D(5)
    Journal of labelled compounds & radiopharmaceuticals
    
    P. Ferraboschi et al., "A FACILE SYNTHESIS OF PENTADEUTERATED DOMIODOL (2-IODOMETHYL-4-HYDROXYMETHYL-1,3-DIOXOLANE) FROM GLYCEROL-1,1,2,3,3-D(5)", Journal of labelled compounds & radiopharmaceuticals, 34(3), 1994, pp. 303-306
11. FERRABOSCHI P; GRISENTI P; MANZOCCHI A; SANTANIELLO E
    BAKERS YEAST-MEDIATED REDUCTION OF ALPHA-HYDROXY KETONES AND DERIVATIVES - THE STERIC COURSE OF THE BIOTRANSFORMATION
    Tetrahedron
    
    P. Ferraboschi et al., "BAKERS YEAST-MEDIATED REDUCTION OF ALPHA-HYDROXY KETONES AND DERIVATIVES - THE STERIC COURSE OF THE BIOTRANSFORMATION", Tetrahedron, 50(35), 1994, pp. 10539-10548
12. FERRABOSCHI P; CASATI S; GRISENTI P; SANTANIELLO E
    SELECTIVE ENZYMATIC TRANSFORMATIONS OF ITACONIC ACID-DERIVATIVES - ANACCESS TO POTENTIALLY USEFUL BUILDING-BLOCKS
    Tetrahedron
    
    P. Ferraboschi et al., "SELECTIVE ENZYMATIC TRANSFORMATIONS OF ITACONIC ACID-DERIVATIVES - ANACCESS TO POTENTIALLY USEFUL BUILDING-BLOCKS", Tetrahedron, 50(10), 1994, pp. 3251-3258
13. GRISENTI P; FERRABOSCHI P; CASATI S; SANTANIELLO E
    STUDIES ON THE ENANTIOSELECTIVITY OF THE TRANSESTERIFICATION OF 2-METHYL-1,4-BUTANEDIOL AND ITS DERIVATIVES CATALYZED BY PSEUDOMONAS-FLUORESCENS LIPASE IN ORGANIC-SOLVENTS
    Tetrahedron : asymmetry
    
    P. Grisenti et al., "STUDIES ON THE ENANTIOSELECTIVITY OF THE TRANSESTERIFICATION OF 2-METHYL-1,4-BUTANEDIOL AND ITS DERIVATIVES CATALYZED BY PSEUDOMONAS-FLUORESCENS LIPASE IN ORGANIC-SOLVENTS", Tetrahedron : asymmetry, 4(5), 1993, pp. 997-1006
14. SANTANIELLO E; FERRABOSCHI P; GRISENTI P
    LIPASE-CATALYZED TRANSESTERIFICATION IN ORGANIC-SOLVENTS - APPLICATIONS TO THE PREPARATION OF ENANTIOMERICALLY PURE COMPOUNDS
    Enzyme and microbial technology
    
    E. Santaniello et al., "LIPASE-CATALYZED TRANSESTERIFICATION IN ORGANIC-SOLVENTS - APPLICATIONS TO THE PREPARATION OF ENANTIOMERICALLY PURE COMPOUNDS", Enzyme and microbial technology, 15(5), 1993, pp. 367-382