Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions.6. Phenoxyacetamido iso-azapenem and iso-azacephem carboxylic acids.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Diastereoselective route to novel fused or bridged tricyclic beta-lactams through intramolecular nitrone-alkene cycloaddition of 2-azetidinone-tethered alkenylaldehydes - Synthetic applications to carbacephams and cyclic beta-amino acid derivatives;EUR J ORG CHEM;2005
2. Diastereoselective Route to Novel Fused or Bridged Tricyclic β-Lactams through Intramolecular Nitrone-Alkene Cycloaddition of 2-Azetidinone-Tethered Alkenylaldehydes - Synthetic Applications to Carbacephams and Cyclic β-Amino Acid Derivatives;European Journal of Organic Chemistry;2005-04
3. Rapid entry to enantiopure polycyclic β-lactams via intramolecular nitrone-alkene cycloaddition of 2-azetidinone-tethered alkenylaldehydes;Tetrahedron Letters;1999-07
4. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996
5. Other Fused Azetidines, Azetines, and Azetes;Comprehensive Heterocyclic Chemistry II;1996
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