Diastereoselective ring - Opening of 12-acetoxy-9α and 9β(11)-epoxy-7-drimene: Homochiral semisynthesis of poligodial and warburganal

DOI: 10.1016/S0040-4039(00)73098-X

Source and publish data:

Tetrahedron Letters p. 3781 - 3784 (1994)

Update date:2022-08-10

Topics:

Authors:

Urones, Julio G.

Marcos, Isidro S.

Gomez-Perez, Belen

Lithgow, Anna M.

Diez, David

Basabe, Pilar

Gomez, Patricio M.

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Article abstract of DOI:10.1016/S0040-4039(00)73098-X

Starting from a zamoranic acid derivative (Methyl 15-tetrahydropiranyloxy-7-labden-17-oate) poligodial and warburganal have been synthesized in several steps with a 55% overall yield and 27% overall yield, respectively.

Full text of DOI:10.1016/S0040-4039(00)73098-X

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Product name:Warburganal

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