Synthetic Studies directed towards the Vancomycin Carboxylate Binding Pocket

DOI: 10.1039/c39920001693

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1693 - 1695 (1992)

Update date:2022-08-03

Topics:

Authors:

Lamont, R. Brian

Allen, David G.

Clemens, Ian R.

Newall, Christopher E.

Ramsay, Michael V. J.

et al. et al.

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Article abstract of DOI:10.1039/c39920001693

The synthesis of the diastereoisomeric lactones 12a and 12b as models for the carboxylate binding pocket of vancomycin is described; the structure of 12a, which corresponds to the diphenyl ether rotamer found in vancomycin, is established by X-ray crystal

Full text of DOI:10.1039/c39920001693

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