Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions. 3.1 6-phenoxyacetamido-7-oxo-1,3-diazabicyclo[3.2.0]heptaine-2-carboxylic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions. Part 2. (8S,8aR)-7,8-dihydro-7-oxo-8-phenoxyacetamido-8aH-azeto[1,2-a]-v-triazolo[3,4-c]pyrimidine-5-carboxylic acids
2. Novel synthesis of the 7-oxo-1,3-diazabicyclo[3.2.0]heptane and 8-oxo-1,3-diazabicyclo[4.2.0]octane ring systems
3. Synthesis of β-lactams through the reaction of mixed anhydrides and imines
4. Total synthesis of dl-antibiotic 593A
5. Nuclear analogs of β-lactam antibiotics. I. Synthesis of O-2-isocephams
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996
2. Other Fused Azetidines, Azetines, and Azetes;Comprehensive Heterocyclic Chemistry II;1996
3. An extension of barret's procedure for the preparation of potentially valuable carbapenem intermediates;Tetrahedron Letters;1988-01
4. Recent Developments in the Field of Cephem Antibiotics;Advances in Drug Research;1988
5. Fused β-lactams via intramolecular dipolar cycloaddition;Tetrahedron Letters;1987-01
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