Absolute Stereochemistry of Proclavaminic Acid, the Monocyclic Biosynthetic Precursor of Clavulanic Acid

DOI: 10.1039/c39880000567

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 567 - 568 (1988)

Update date:2022-08-02

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Authors:

Baggaley, Keith H.

Nicholson, Neville H.

Sime, John T.

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Article abstract of DOI:10.1039/c39880000567

Proclavaminic acid (1) has been synthesized by a route which indicated the absolute stereochemistry of the two chiral centres to be (2S,3R).

Full text of DOI:10.1039/c39880000567

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