Stereoselective epoxidation of hydroxyenones. The synthesis of the sidechain of clerocidin

DOI: 10.1016/S0040-4039(00)97662-7

Source and publish data:

Tetrahedron Letters p. 4509 - 4512 (1990)

Update date:2022-09-26

Topics:

Authors:

Bailey Bailey

Marko Marko

Ollis Ollis

Rasmussen

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Article abstract of DOI:10.1016/S0040-4039(00)97662-7

The sidechains of clerocidin 1 and terpentecin 2 contain a unique chiral assembly [C₅H₅O₄]. Models for the stereospecific synthesis of this structural feature are reported.

Full text of DOI:10.1016/S0040-4039(00)97662-7

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