Studies on penam sulfones III. Synthesis and β-lactamase inhibitory activity of sodium (6R)-6-(α-hydroxybenzyl)-2β-methoxyiminomethyl-2α-methylpenam-3α-carboxylate 1,1-dioxide and sodium 2β-acyl-2α-methylpenam-3α-carboxylate 1,1-dioxide
✍ Scribed by David P Czajkowski; Andhe V.N Reddy; Eduardo L Setti; Oludotun A Phillips; Ronald G Micetich; Chieko Kunugita; Samarendra N Maiti
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 199 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0960-894X
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✦ Synopsis
The synthesis and in vitro synergies of (6R)-6-(~-hydroxybenzyl)-2[~-methoxyiminomethyl-2~methylpenam-30~-carboxylate 1,1-dioxide (4) and 2~-acyl-2~-methylpenam-3ct-carboxylate l,l-dioxide (15) are described. Compound 15 showed good in vitro synergy in combination with piperacillin and ceftazidime against chromosomally mediated class I cephalosporinase producing organisms including TEM, SHV, and OXA-type enzymes producing microorganisms.
📜 SIMILAR VOLUMES
## Abstract The __García‐González__ reaction of D‐glucose and ethyl acetoacetate generated ethyl 5‐[(1′__S__)‐D‐erythrosyl]‐2‐methyl‐3‐furoate (**5**), which was converted to ethyl 5‐[(1′__R__)‐1′,4′‐dideoxy‐1′,4′‐imino‐D‐erythrosyl]‐2‐methyl‐3‐furoate (**3c**) and to ethyl 5‐[(1′__S__)‐1′,4′‐dideo