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Results: 1-12 |
Results: 12
A SHORT, STEREOSELECTIVE SYNTHESIS OF 1'((T-BUTYLDIMETHYLSILYL)OXY)ETHYL]-2-AZETIDINONE, KEY INTERMEDIATE FOR THE PREPARATION OF CARBAPENEMANTIBIOTICS
Authors: COZZI F ANNUNZIATA R CINQUINI M POLETTI L PERBONI A TAMBURINI B
Citation: F. Cozzi et al., A SHORT, STEREOSELECTIVE SYNTHESIS OF 1'((T-BUTYLDIMETHYLSILYL)OXY)ETHYL]-2-AZETIDINONE, KEY INTERMEDIATE FOR THE PREPARATION OF CARBAPENEMANTIBIOTICS, Chirality, 10(1-2), 1998, pp. 91-94
SYNTHESIS AND NMR-STUDIES OF KEY INTERMEDIATES TO A NEW CLASS OF BETA-LACTAM - THE TRINEMS
Authors: MARCHIORO C PENTASSUGLIA G PERBONI A DONATI D
Citation: C. Marchioro et al., SYNTHESIS AND NMR-STUDIES OF KEY INTERMEDIATES TO A NEW CLASS OF BETA-LACTAM - THE TRINEMS, Journal of the Chemical Society. Perkin transactions. I, (4), 1997, pp. 463-468
THE SYNTHESIS OF 4-AMINOCARBONYLMETHOXY TRINEMS
Authors: BERTANI B DIFABIO R GHIRON C PERBONI A ROSSI T THOMAS RJ ZARANTONELLO P
Citation: B. Bertani et al., THE SYNTHESIS OF 4-AMINOCARBONYLMETHOXY TRINEMS, Tetrahedron, 53(44), 1997, pp. 15011-15028
SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 4-METHOXY AND 8-METHOXY TRINEMS
Authors: ANDREOTTI D ROSSI T GAVIRAGHI G DONATI D MARCHIORO C DIMODUGNO E PERBONI A
Citation: D. Andreotti et al., SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 4-METHOXY AND 8-METHOXY TRINEMS, Bioorganic & medicinal chemistry letters, 6(4), 1996, pp. 491-496
HIGHLY STEREOCONTROLLED SYNTHESIS OF ENANTIOMERIC 4-METHOXY TRINEMS VIA RESOLUTION OF SCALEMIC ENOL PHOSPHATES
Authors: PANUNZIO M CAMERINI R PACHERA R DONATI D MARCHIORO C PERBONI A
Citation: M. Panunzio et al., HIGHLY STEREOCONTROLLED SYNTHESIS OF ENANTIOMERIC 4-METHOXY TRINEMS VIA RESOLUTION OF SCALEMIC ENOL PHOSPHATES, Tetrahedron : asymmetry, 7(10), 1996, pp. 2929-2938
SYNTHESIS OF ESTERS OF THE POTENT ANTIBACTERIAL TRINEMS AND ANALOGS
Authors: JACKSON PM ROBERTS SM DAVALLI S DONATI D MARCHIORO C PERBONI A PROVIERA S ROSSI T
Citation: Pm. Jackson et al., SYNTHESIS OF ESTERS OF THE POTENT ANTIBACTERIAL TRINEMS AND ANALOGS, Journal of the Chemical Society. Perkin transactions. I, (16), 1996, pp. 2029-2039
HIGHLY STEREOCONTROLLED SYNTHESIS OF A NOVEL TRIBACTAM BY REACTION OFAN ESTER ENOLATE WITH A N-TRIMETHYLSILYLIMINE
Authors: CAMERINI R PANUNZIO M BONANOMI G DONATI D PERBONI A
Citation: R. Camerini et al., HIGHLY STEREOCONTROLLED SYNTHESIS OF A NOVEL TRIBACTAM BY REACTION OFAN ESTER ENOLATE WITH A N-TRIMETHYLSILYLIMINE, Tetrahedron letters, 37(14), 1996, pp. 2467-2470
SYNTHESIS OF A NOVEL FLUORO-TRIBACTAM UTILIZING AN N-FLUOROSULFONIMIDE IN THE KEY STEP
Authors: PADOVA A ROBERTS SM DONATI D MARCHIORO C PERBONI A
Citation: A. Padova et al., SYNTHESIS OF A NOVEL FLUORO-TRIBACTAM UTILIZING AN N-FLUOROSULFONIMIDE IN THE KEY STEP, Tetrahedron, 52(1), 1996, pp. 263-270
SYNTHESIS AND ANTIMICROBIAL EVALUATION OF ETA-CARBAMOYLMETHYL-PENAM-1,1-DIOXIDE-3-CARBOXYLIC ACID
Authors: GAVIRAGHI G PERBONI A TAMBURINI B XERRI L SALVATORI A SPADONI G TARZIA G
Citation: G. Gaviraghi et al., SYNTHESIS AND ANTIMICROBIAL EVALUATION OF ETA-CARBAMOYLMETHYL-PENAM-1,1-DIOXIDE-3-CARBOXYLIC ACID, Il Farmaco, 51(7), 1996, pp. 535-538
SYNTHESIS OF A NOVEL FLUORO-TRIBACTAM UTILIZING N-FLUOROSULFONIMIDE IN THE KEY STEP
Authors: PADOVA A ROBERTS SM DONATI D MARCHIORO C PERBONI A
Citation: A. Padova et al., SYNTHESIS OF A NOVEL FLUORO-TRIBACTAM UTILIZING N-FLUOROSULFONIMIDE IN THE KEY STEP, Journal of the Chemical Society, Chemical Communications, (6), 1995, pp. 661-662
SYNTHESIS OF NOVEL 6-ALPHA AND 6-BETA-ALKYLCARBONYLMETHYL SUBSTITUTEDPENEMS
Authors: PENTASSUGLIA G TARZIA G ANDREOTTI D BISMARA C CARLESSO R DONATI D GAVIRAGHI G PERBONI A PEZZOLI A ROSSI T TAMBURINI B URSINI A
Citation: G. Pentassuglia et al., SYNTHESIS OF NOVEL 6-ALPHA AND 6-BETA-ALKYLCARBONYLMETHYL SUBSTITUTEDPENEMS, Journal of antibiotics, 48(5), 1995, pp. 399-407
CARBON-CARBON BOND FORMATION AT THE C-4 POSITION OF AN AZETIDIN-2-ONERING BY INTERMOLECULAR RADICAL COUPLING REACTIONS - A ROUTE TO TRIBACTAMS
Authors: PADOVA A ROBERTS SM DONATI D PERBONI A ROSSI T
Citation: A. Padova et al., CARBON-CARBON BOND FORMATION AT THE C-4 POSITION OF AN AZETIDIN-2-ONERING BY INTERMOLECULAR RADICAL COUPLING REACTIONS - A ROUTE TO TRIBACTAMS, Journal of the Chemical Society, Chemical Communications, (4), 1994, pp. 441-442
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