Rearrangement of an Isothiazolidinone to a β-Lactam. A Model for Penicillin Biosynthesis

DOI: 10.1039/c39830001349

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1349 - 1350 (1983)

Update date:2022-08-05

Topics:: Authors:

Easton, Christopher J.

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Article abstract of DOI:10.1039/c39830001349

Based on novel syntheses of a β-lactam from an isothiazolidinone, a mechanism of formation of the β-lactam ring in penicillin biosynthesis is proposed.

Full text of DOI:10.1039/c39830001349

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Rearrangement of an Isothiazolidinone to a β-Lactam. A Model for Penicillin Biosynthesis

DOI: 10.1039/c39830001349

Source and publish data:

Authors:

Article abstract of DOI:10.1039/c39830001349

Full text of DOI:10.1039/c39830001349

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