Chlorosphaeropsidone and Epichlorospaeropsidone, Two New Chlorinated Dimedone Methyl Ethers Isolated from Liquid Cultures of «Sphaeropsis sapinea» f. sp. «cupressi»
Abstract
Two new dimedone methyl ethers, named chlorosphaeropsidone and epichlorosphaeropsidone were isolated
from the culture filtrates of Sphaeropsis sapinea f. sp. cupressi, the causal agent of a canker of Italian cypress
(Cupressus sempervirens L.). The same fungus also produced various phytotoxic metabolites: three pimarane diterpenes
(sphaeropsidins A, B and C) and two dimedone methyl ethers (sphaeropsidone and episphaeropsidone).
Chlorosphaeropsidone and epichlorosphaeropsidone were characterized using chemical and spectroscopic methods
as two 6-chloro-4,5-dihydroxy-3-methoxycyclohex-2-en-1-ones epimers at C-6. Their relative and absolute configurations
were established by NMR, X-ray analysis and circular dichroism. Assayed on host plants they did not show
phytotoxic activity. Comparison with other sphaeropsidones suggested that this might result from opening of the
epoxy ring.
from the culture filtrates of Sphaeropsis sapinea f. sp. cupressi, the causal agent of a canker of Italian cypress
(Cupressus sempervirens L.). The same fungus also produced various phytotoxic metabolites: three pimarane diterpenes
(sphaeropsidins A, B and C) and two dimedone methyl ethers (sphaeropsidone and episphaeropsidone).
Chlorosphaeropsidone and epichlorosphaeropsidone were characterized using chemical and spectroscopic methods
as two 6-chloro-4,5-dihydroxy-3-methoxycyclohex-2-en-1-ones epimers at C-6. Their relative and absolute configurations
were established by NMR, X-ray analysis and circular dichroism. Assayed on host plants they did not show
phytotoxic activity. Comparison with other sphaeropsidones suggested that this might result from opening of the
epoxy ring.
Firenze University Press
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E-mail: journals@fupress.com
Borgo Albizi, 28 - 50122 Firenze
Tel. (0039) 055 2743051 Fax (0039) 055 2743058
E-mail: journals@fupress.com



