Desulphurative approaches to penem antibiotics. V. 2-(Functionalized methyl)penems from 3-methylenecepham-1-oxides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Desulphurative approaches to penem antibiotics. III. Synthesis and desulphurisation of 3-methyl-2-thiacephem-4-carboxylates
2. Conversion of cepham-1-oxide into 1-oxadethiacepham
3. Desulphurative approaches to penem antibiotics. IV. Bromination of 3-methyl-2-thiacephems, a novel entry in the synthesis of potent antimicrobial agents
4. Biological activity of (5R,6S,8R)-6-.ALPHA.-hydroxyethyl-2-acetoxymethyl-2-penem-3-carboxylate.
5. 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 22891.
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1. Synthesis of Fused 1,2,4-Dithiazines and 1,2,3,5-Trithiazepines;The Journal of Organic Chemistry;2014-10-02
2. Development of a Second-Generation Process to Antibacterial Candidate Sulopenem;Organic Process Research & Development;2012-07-31
3. An Industrial Perspective on Total Synthesis; Penem Antibacterial CP-70,429;Strategies and Tactics in Organic Synthesis;1991
4. Rearrangement of unsym-azetidinone disulphides to 2β-(thio-substituted methyl) penams;Tetrahedron Letters;1990-01
5. Synthesis of Penems;Recent Progress in the Chemical Synthesis of Antibiotics;1990
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