A new synthetic route to 7 α-methoxycephalosporins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. A new semisynthetic 7.ALPHA.-methoxycephalosporin, CS-1170. 7.BETA.-(((cyanomethyl)thio)acetamido)-7.ALPHA.-methoxy-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid.
2. Synthesis and in vitro antibacterial activity of 7-trifluoromethylthioacetamido cephamycins related to SK&F59962(cefazaflur).
3. Diastereomeric 7-ureidoacetyl cephalosporins. II. 7.BETA.[[[(Aminocarbonyl) amino]-2-thienylacetyl] amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl) thio] methyl]-8-oxo-5-thia-1-azabicyclo [4.2.0] oct-2-ene-2-carboxylic acid.
4. Sulfenyl transfer rearrangement of thiooximes. A novel conversion of cephalosporins to 7.alpha.-methoxycephalosporins
5. A novel synthetic route to 7.ALPHA.-methoxycephalosporins.
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1. A Study of New Synthetic Reaction for Industrial Production: A Synthetic Route to Cephamycins (7.ALPHA.-Methoxycephalosporins);Journal of Synthetic Organic Chemistry, Japan;2011
2. Synthesis and Reactivity of Novel α,α,β- and α,α,δ-Trichlorinated Imines;Synlett;2008-09-10
3. Research and Process Development of Cefditoren Pivoxil: An Oral Cephalosporin Antibiotic.;Journal of Synthetic Organic Chemistry, Japan;2002
4. Synthesis of cefminox by cell-free extracts ofStreptomyces clavuligerus;FEMS Microbiology Letters;2000-01
5. Synthesis of functionalised cephalosporins;Tetrahedron;1985-01
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