Author:
Cambie Richard C.,Liu Carrie C.,Rickard Clifford E. F.,Rutledge Peter S.
Abstract
The structure of a naphthalene derivative obtained by rearrangement of
13-methoxytotara-5,8,11,13-tetraen-7α-ol (2) has been revised to
5-(5′-isopropyl-6′-methoxy-2′-methyl-1′-naphthyl)-2-methylpent-2-ene
(7). A minor oxidation product of 13-methoxytotara-8,11,13-triene (4) has been
identified as
4-methoxy-3,3-dimethyl-7-(1′,3′,3′-trimethyl-2′-oxocyclohexanyl)isobenzofuran-1(3H)-one
(16) and its structure confirmed by X-ray crystallography. Methyl
12-methoxypodocarpa-8,11,13-trien-19-oate (12) has been converted into an
intermediate used in the synthesis of the linear diterpenoid umbrosone
[3-(1′-hydroxy-1′-methylethyl)-5,5,9-trimethyl-5,6,7,8-tetrahydroanthracene-1,2-dione]
(15).
Cited by
4 articles.
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