Stereoselective synthesis of Macrolactin A analogues. Part 2: The C1-C14 fragment

DOI: 10.1016/0040-4020(96)00667-9

Source and publish data:

Tetrahedron p. 11821 - 11826 (1996)

Update date:2022-08-02

Topics:

Authors:

Benvegnu, Thierry J.

Gree, Rene L.

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Article abstract of DOI:10.1016/0040-4020(96)00667-9

A synthetic approach to the C₁-C₁₄ part of Macrolactin A analogues is presented. The sequence involving hydroboration-Pd° coupling reaction was found to be the most efficient in term of chemio- and stereo-selectivity to prepare the sensitive and functionalized E,Z diene unit.

Full text of DOI:10.1016/0040-4020(96)00667-9

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