Perfumes 1994
DOI: 10.1007/978-94-011-3826-0_7
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Trapping, Investigation and Reconstitution of Flower Scents

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1994
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Cited by 41 publications
(46 citation statements)
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“…(E)-DMNT is a common constitutively produced floral terpene (Kaiser, 1991;Azuma et al, 1997) and is also induced in response to herbivore damage of foliage in gymnosperms (Su et al, 2009) and in many monocot and dicot angiosperm plant species (Bouwmeester et al, 1999;Arimura et al, 2000Arimura et al, , 2008Degenhardt and Gershenzon, 2000;Kant et al, 2004;Lee et al, 2010). However, (E)-DMNT is not generally detected from undamaged or mechanically damaged foliage.…”
Section: Discussion Volatile Terpene Production In CV Royal Gala Appementioning
confidence: 99%
“…(E)-DMNT is a common constitutively produced floral terpene (Kaiser, 1991;Azuma et al, 1997) and is also induced in response to herbivore damage of foliage in gymnosperms (Su et al, 2009) and in many monocot and dicot angiosperm plant species (Bouwmeester et al, 1999;Arimura et al, 2000Arimura et al, , 2008Degenhardt and Gershenzon, 2000;Kant et al, 2004;Lee et al, 2010). However, (E)-DMNT is not generally detected from undamaged or mechanically damaged foliage.…”
Section: Discussion Volatile Terpene Production In CV Royal Gala Appementioning
confidence: 99%
“…The introduction of gas chromatography in the 1960s was a key step towards better characterizing essential oils for their constituents and odoriferous ingredients. The investigation of raw materials and, if needed, the reconstitutions of flower scents has greatly gained from the advancements of analytical techniques and ultimately allowed the application of headspace techniques for the investigation and subsequent reconstitution of all sorts of natural scents (Kaiser 1991). The identification of the first new natural products by this new analytical approach goes back to 1978-1979 and has been reported almost 30 years ago (Kaiser and Lamparsky 1980) when several oximes were described.…”
Section: Natural Scentsmentioning
confidence: 99%
“…We have shown that the strong, sweet fragrance of C. breweri consists of some 8 to 12 different volatiles that fall into two groups: monoterpenoids and benzenoids (Raguso and Pichersky, 1994). A major component of the scent is linalool, an acyclic monoterpene common to the floral scents of numerous other plant species (Kaiser, 1991;Knudsen et al, 1993). Two cyclic isomers of linalool oxide are also produced by C. breweri (Fig.…”
mentioning
confidence: 98%
“…Most of these compounds are either terpenoids, benzenoid compounds, or acyl lipid derivatives (Croteau and Karp, 1991). Although perfumers still survey natural sources for novel fragrance compounds (Joulain, 1987;Kaiser, 1991), this information is most often used in directing organic syntheses to imitate natural fragrances or create new combinations. Thus, although the structures of many floral scent compounds are known, very few studies have focused on the biosyntheses of these compounds in the plant cell.…”
mentioning
confidence: 99%