The stereoselective synthesis of a key intermediate of the trinem antibiotic Sanfetrinem

DOI: 10.1016/0040-4039(96)00682-X

Source and publish data:

Tetrahedron Letters p. 3891 - 3894 (1996)

Update date:2022-08-05

Topics:

Authors:

Ghiron, Chiara

Piga, Elisabetta

Rossi, Tino

Tamburini, Bruno

Thomas, Russell J.

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Article abstract of DOI:10.1016/0040-4039(96)00682-X

By modulating the reactivity of the Lewis acid promoter it was possible to obtain, in a single stereoselective condensation step, the methoxyketone 7, an advanced intermediate in the synthesis of Sanfetrinem GV 104326.

Full text of DOI:10.1016/0040-4039(96)00682-X

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