2-Acetamidoethenylthioesters have been prepared from 4-carboxymethylazetidin-2-one and cyclised via an intramolecular Wittig reaction to provide 3-(2-acetamidoethenylthio)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates, closely related analogues of the naturally occurring antibiotic MM 13902 (1).

This study successfully synthesized 3-(2-acetamidoethenylthio)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates, closely related analogues of the naturally occurring antibiotic MM 13902, using 4-

Journal of The Chemical Society, Chemical Communications

Synthesis of olivanic acid analogues. Preparation of 7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates containing the 3-(2-acetamidoethenylthio) side chain

Paper

Synthesis of olivanic acid analogues. Preparation of 7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates containing the 3-(2-acetamidoethenylthio) side chain

References

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