Towards the total synthesis of clerodin. Part II

DOI: 10.1016/S0040-4039(00)79436-6

Source and publish data:

Tetrahedron Letters p. 5957 - 5958 (1991)

Update date:2022-07-29

Topics:

Authors:

Bouchard

Soulie Soulie

Lallemand

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Article abstract of DOI:10.1016/S0040-4039(00)79436-6

In a model study aimed at the total synthesis of clerodin 1, the tricyclic furo-furan moiety 2 was prepared. This approach was based on a stereoselective Claisen rearrangement between a cyclohexenol and a cyclic orthoester.

Full text of DOI:10.1016/S0040-4039(00)79436-6

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