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A Bedeschi

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The Journal of Antibiotics|June 1, 1982
Cephalosporins. V. Synthesis and in vitro activity of some 7-[2-methoxyimino-(substituted thio)alkanoyl]amino cephalosporanic acid derivativesA Bedeschi, A Crugnola, F Giudici, et al.
The Journal of Antibiotics|April 1, 1981
Cephalosporins. II. Synthesis and structure-activity relationships of new 7-vinylenethioacetamido and thioacrylamido cephalosporinsG Nannini, E Perrone, D Severino, et al.
The Journal of Antibiotics|May 1, 1992
Synthesis and biological properties of FCE 25199, a new oral penemM Alpegiani, A Bedeschi, F Zarini, et al.
The Journal of Antimicrobial Chemotherapy|March 1, 1989
Synthesis and antimicrobial spectrum of FCE 22101 and its orally available ester FCE 22891G Franceschi, E Perrone, M Alpegiani, et al.
The Journal of Antibiotics|July 1, 1988
Structure determination of the primary renal metabolite of the penem FCE 22101G Cassinelli, R Corigli, P Orezzi, et al.
The Journal of Antibiotics|June 1, 1984
A new class of penems, the 2-heterocyclyl(thio)methyl derivativesG Franceschi, M Alpegiani, A Bedeschi, et al.
The Journal of Antibiotics|September 1, 1986
2-(quaternary ammonio)-methyl penemsE Perrone, M Alpegiani, A Bedeschi, et al.
The Journal of Antibiotics|November 1, 1987
Novel quaternary ammonium penems: the [(pyridinio)methyl]-phenyl derivativesE Perrone, M Alpegiani, A Bedeschi, et al.
The Journal of Antibiotics|March 1, 1990
Synthesis and structure-activity relations in the class of 2-(pyridyl)penemsA Bedeschi, G Visentin, E Perrone, et al.
The Journal of Antibiotics|July 1, 1983
Synthesis and biological properties of sodium (5R, 6S, 8R)-6 alpha-hydroxyethyl-2-carbamoyloxymethyl-2-penem-3-carboxylate (FCE 22101) and its orally absorbed esters FCE 22553 and FCE 22891G Franceschi, M Foglio, M Alpegiani, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Journal of Antibiotics|June 1, 1982
Cephalosporins. V. Synthesis and in vitro activity of some 7-[2-methoxyimino-(substituted thio)alkanoyl]amino cephalosporanic acid derivativesA Bedeschi, A Crugnola, F Giudici, et al.
The Journal of Antibiotics|April 1, 1981
Cephalosporins. II. Synthesis and structure-activity relationships of new 7-vinylenethioacetamido and thioacrylamido cephalosporinsG Nannini, E Perrone, D Severino, et al.
The Journal of Antibiotics|May 1, 1992
Synthesis and biological properties of FCE 25199, a new oral penemM Alpegiani, A Bedeschi, F Zarini, et al.
The Journal of Antimicrobial Chemotherapy|March 1, 1989
Synthesis and antimicrobial spectrum of FCE 22101 and its orally available ester FCE 22891G Franceschi, E Perrone, M Alpegiani, et al.
The Journal of Antibiotics|July 1, 1988
Structure determination of the primary renal metabolite of the penem FCE 22101G Cassinelli, R Corigli, P Orezzi, et al.
The Journal of Antibiotics|June 1, 1984
A new class of penems, the 2-heterocyclyl(thio)methyl derivativesG Franceschi, M Alpegiani, A Bedeschi, et al.
The Journal of Antibiotics|September 1, 1986
2-(quaternary ammonio)-methyl penemsE Perrone, M Alpegiani, A Bedeschi, et al.
The Journal of Antibiotics|November 1, 1987
Novel quaternary ammonium penems: the [(pyridinio)methyl]-phenyl derivativesE Perrone, M Alpegiani, A Bedeschi, et al.
The Journal of Antibiotics|March 1, 1990
Synthesis and structure-activity relations in the class of 2-(pyridyl)penemsA Bedeschi, G Visentin, E Perrone, et al.
The Journal of Antibiotics|July 1, 1983
Synthesis and biological properties of sodium (5R, 6S, 8R)-6 alpha-hydroxyethyl-2-carbamoyloxymethyl-2-penem-3-carboxylate (FCE 22101) and its orally absorbed esters FCE 22553 and FCE 22891G Franceschi, M Foglio, M Alpegiani, et al.
Pageof 2