• Thumbnail for Jasmone
    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...
    3 KB (173 words) - 22:14, 11 July 2024
  • Thumbnail for Cyclopentanone
    common precursor to fragrances, especially those related to jasmine and jasmone. Examples include 2-pentyl- and 2-heptylcyclopentanone. It is a versatile...
    5 KB (221 words) - 12:13, 27 August 2023
  • Thumbnail for Bombyx mori
    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...
    37 KB (4,240 words) - 05:18, 10 August 2024
  • The molecular formula C11H16O may refer to: Jasmone Various aromatic alcohols with one benzene ring Various aromatic ethers such as benzyl tert-butyl...
    392 bytes (67 words) - 12:06, 9 January 2022
  • Thumbnail for Aroma compound
    woody Violet Thujone Minty Wormwood, lilac, juniper Eucalyptol Eucalyptus Eucalyptus Jasmone spicy, fruity, floral in dilution Jasmine, Honeysuckle...
    21 KB (1,542 words) - 03:14, 15 July 2024
  • ubiquity of cyclopentenones as both motifs in natural products (including jasmone, the aflatoxins, and a subclass of prostaglandins) and as useful synthetic...
    25 KB (2,696 words) - 13:46, 4 July 2023
  • Cyclopentenones are found in a large number of natural products, including jasmone, the aflatoxins, and several prostaglandins. 2-Cyclopentenones can be synthesized...
    6 KB (534 words) - 15:11, 27 November 2023
  • Thumbnail for Jasmonic acid
    some biological contexts. Decarboxylation affords the related fragrance jasmone. Demole, E.; Lederer, E.; Mercier, D. (1962). "Isolement et determination...
    11 KB (1,125 words) - 22:20, 11 July 2024
  • Thumbnail for Jasmonate
    nigrum's herbivore resistance. JA undergoes decarboxylation to give cis-jasmone. Although jasmonate (JA) regulates many different processes in the plant...
    23 KB (2,887 words) - 22:51, 13 June 2024
  • Thumbnail for Cereal leaf beetle
    ; Lemanczyk, G.; Wrzesinska, D.; Piesik, D. (May 2013). "Synthetic cis-jasmone exposure induces wheat and barley volatiles that repel the pest cereal...
    23 KB (2,743 words) - 03:39, 17 July 2024
  • Thumbnail for Jasmine in Karnataka
    from 0.24 to 0.42 per cent. The principal aromatic components are Indol, Jasmone, Benzyl Acetate, Benzyl Benzoate, Methyl Anthranilate, Linalool & Geraniol...
    22 KB (2,716 words) - 19:22, 9 July 2024
  • Thumbnail for Floral scent
    2009). "Attraction of New Zealand Flower Thrips, Thrips obscuratus, to cis-Jasmone, a Volatile Identified from Japanese Honeysuckle Flowers". Journal of Chemical...
    25 KB (3,145 words) - 02:50, 3 December 2023
  • Thumbnail for Nikolay Zefirov
    anhydride. Later these transformations have found applications for the trans-Jasmone synthesis. It is noteworthy that all research work of this time was conducted...
    16 KB (1,590 words) - 02:10, 2 April 2024
  • considerably bigger than the typical jar in English today. jasmine, jessamine, jasmone ياسمين yās(a)mīn, jasmine[jaːsmjn] (listen). In medieval Arabic jasmine...
    60 KB (7,207 words) - 00:23, 15 October 2023