Issue 6, 1998

The 1,3-Dipolar Cycloaddition Reaction of 7,14-Dioxa-1-azadispiro[4.2.5.2]pentadec-1-ene 1-Oxide Derivatives with N-Phenylmaleimide. An Attempt to Synthesize Azasugar Analogues of Showdomycine

Abstract

7,14-Dioxa-1-azadispiro[4.2.5.2]pentadec-1-ene 1-oxide derivatives (1) undergo 1,3-dipolar cycloaddition reaction with N-phenylmaleimide (2) giving the corresponding isoxazolidines (3); attempts to convert 3 into the showdomycine azasugar analogues A and B failed.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 298-299

The 1,3-Dipolar Cycloaddition Reaction of 7,14-Dioxa-1-azadispiro[4.2.5.2]pentadec-1-ene 1-Oxide Derivatives with N-Phenylmaleimide. An Attempt to Synthesize Azasugar Analogues of Showdomycine

M. Koszytkowska-Stawin′ska and W. Sas, J. Chem. Res. (S), 1998, 298 DOI: 10.1039/A706366K

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