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Jasmone is an
organic compound,
which is a
volatile portion of the oil from
jasmine flowers. It is a
colorless to pale
yellow liquid.
Jasmone can exist...
-
common precursor to fragrances,
especially those related to
jasmine and
jasmone.
Examples include 2-pentyl- and 2-heptylcyclopentanone. It is a versatile...
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woody Violet Thujone Minty Wormwood, lilac,
juniper Eucalyptol Eucalyptus Eucalyptus Jasmone ****y, fruity,
floral in
dilution Jasmine, Honeysuckle...
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ubiquity of
cyclopentenones as both
motifs in
natural products (including
jasmone, the aflatoxins, and a
subclass of prostaglandins) and as
useful synthetic...
-
preference for
white mulberry,
having an
attraction to the
mulberry odorant cis-
jasmone. They are not monophagous,
since they can eat
other species of Morus, as...
-
Cyclopentenones are
found in a
large number of
natural products,
including jasmone, the aflatoxins, and
several prostaglandins. 2-Cyclopentenones can be synthesized...
- ; Lemanczyk, G.; Wrzesinska, D.; Piesik, D. (May 2013). "Synthetic cis-
jasmone exposure induces wheat and
barley volatiles that
repel the pest cereal...
- some
biological contexts.
Decarboxylation affords the
related fragrance jasmone. Demole, E.; Lederer, E.; Mercier, D. (1962). "Isolement et determination...
- nigrum's
herbivore resistance. JA
undergoes decarboxylation to give cis-
jasmone.
Although jasmonate (JA)
regulates many
different processes in the plant...
- from 0.24 to 0.42 per cent. The prin****l
aromatic components are Indol,
Jasmone,
Benzyl Acetate,
Benzyl Benzoate,
Methyl Anthranilate,
Linalool & Geraniol...
