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PINESCHI, MAURO Statistiche

PINESCHI, MAURO  

DIPARTIMENTO DI FARMACIA  

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Titolo Data di pubblicazione Autore(i) File
1,3-DIAZO-4-OXA-[3.3.1]-BICYCLIC DERIVATIVES, PROCESS FOR THEIR MANUFACTURE AND THEIR USE AS A MEDICAMENT, IN PARTICULAR FOR TREATING DIABETES 1-gen-2018 Berti, Francesco; Pineschi, Mauro; Menichetti, Andrea
1,3-DIAZO-4-OXA-[3.3.1]-BICYCLIC DERIVATIVES,PROCESS FOR THEIR MANUFACTURE AND THEIR USE AS A MEDICAMENT, IN PARTICULAR FOR TREATING DIABETES 1-gen-2019 Pineschi, Mauro; Berti, Francesco; Menichetti, Andrea
1,3-DIAZO-4-OXA-[3.3.1]-BICYCLIC DERIVATIVES,PROCESS FOR THEIR MANUFACTURE AND THEIR USE AS A MEDICAMENT, IN PARTICULAR FOR TREATING DIABETES 1-gen-2019 Pineschi, Mauro
7 Borylative Ring Opening 1-gen-2019 Pineschi, Mauro
A Multigram, Catalytic and Enantioselective Synthesis of Opitically Active 4-Methyl-2-ciyclohexen-1-one: a Useful Chiral Building Block 1-gen-2001 Bertozzi, F.; Crotti, Paolo; Feringa, B. L.; Macchia, F; Pineschi, Mauro
A New Catalytic and Enantioselective Desymmetrization of Symmetrical Methylidene Cycloalkene Oxides 1-gen-2000 F., Bertozzi; Crotti, Paolo; F., Macchia; Pineschi, Mauro; A., Arnold; E. B. L., Feringa
A new diastereo- and enantioselective copper-catalyzed conversion of alkynyl epoxides into alpha-allenic alcohols. 1-gen-1999 Bertozzi, F; Crotti, Paolo; Macchia, F; Pineschi, Mauro; Arnold, A; Feringa, Bl
A new regio- and stereoselective intermolecular Friedel-Crafts alkylation of phenolic substrates with aryl epoxides 1-gen-2006 Bertolini, F.; Crotti, Paolo; Macchia, F; Pineschi, Mauro
A novel effective transition metal based salt-catalyzed azidolysis of 1,2-epoxides 1-gen-1996 Crotti, Paolo; DI BUSSOLO, Valeria; Favero, Lucilla; F., Macchia; Pineschi, Mauro
A Practical Regioselective Ring Opening of Activated Aziridines with Organoalanes 1-gen-2009 F., Bertolini; S., Woodward; S., Crotti; Pineschi, Mauro
Addizioni asimmetriche catalitiche di C-nucleofili ad accettori insaturi 1-gen-2000 Pineschi, Mauro
Advances in the Ring Opening of Small-Ring Heterocycles with Organoboron Derivatives 1-gen-2014 Pineschi, Mauro
Allil epossidi derivati da glicali in processi reiterativi di O-glicosilazione stereoselettiva per la sintesi di 1,6-oligosaccaridi 2,3-insaturi 1-gen-2006 DI BUSSOLO, Valeria; M. R., Romano; Pineschi, Mauro; Crotti, Paolo
Aminolysis of Glycal-Derived Allyl Epoxides and Activated Aziridines. Effects of the Absence of Coordination Processes on the Regio- and Stereoselectivity, 1-gen-2010 DI BUSSOLO, Valeria; Favero, Lucilla; Pineschi, Mauro; Crotti, Paolo; L., Checchia; M. R., Romano
AMINOLYSIS OF OXETANES - QUITE EFFICIENT CATALYSIS BY LANTHANIDE(III) TRIFLUOROMETHANSULFONATES 1-gen-1994 Crotti, Paolo; Favero, Lucilla; Macchia, F; Pineschi, Mauro
An efficient stereoselective synthesis of enantiomerically pure aziridine derivatives of allyl beta-D-glucopyranosides asymmetrically induced by a glucide moiety 1-gen-1998 Chiappe, Cinzia; Crotti, Paolo; Menichetti, E; Pineschi, Mauro
An efficient stereoselective synthesis of the amino sugar component (E ring) of calicheamicin gamma(I)(1) 1-gen-1996 Crotti, Paolo; DI BUSSOLO, Valeria; Favero, Lucilla; F., Macchia; Pineschi, Mauro
Aromatic substituent effect on the stereoselectivity of the condensed- and gas-phase acid-induced methanolysis in 2-aryloxiranes derived from 3,4-dihydronaphthalene and trans-1,2,3,4,4a,10a-hexahydrophenanthrene bearing a tertiary benzylic oxirane nucleophilic center 1-gen-1997 Crotti, Paolo; DI BUSSOLO, Valeria; Favero, Lucilla; Pineschi, Mauro; D., Sergiampietri; G., Renzi; M., Ricciutelli; G., Roselli
Asymmetric Ring Opening of Epoxides and Aziridines with Carbon Nucleophiles 1-gen-2006 Pineschi, Mauro
Asymmetric Synthesis of Methylphenidate and Quinolizidinones by Addition of Aldehydes to Piperidine-Based Conjugated N -Acyl-iminium Ions 1-gen-2016 Berti, Francesco; Favero, Lucilla; Pineschi, Mauro