Chirality and biosynthesis of lilac compounds in Actinidia arguta flowers

Phytochemistry

Volumn 68, Issue 13, 2007, Pages 1746-1751

  Matich, A J ^a   Bunn, B J ^a   Comeskey, D J ^a   Hunt, M B ^a   Rowan, D D ^a  

^a THE NEW ZEALAND INSTITUTE FOR PLANT AND FOOD RESEARCH LIMITED   (New Zealand)

Author keywords

8 Hydroxylinalool; 8 Oxolinalool; Actinidia arguta; Deuterium labelling; Enantioselective GC MS; Lilac alcohol epoxides; Lilac alcohols; Lilac aldehydes; Linalool; Monoterpenes

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE; DEUTERIUM; LINALOOL; TERPENE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; FLOWER; KIWIFRUIT; MASS FRAGMENTOGRAPHY; METABOLISM; STEREOISOMERISM;

ACTINIDIA; ALCOHOLS; ALDEHYDES; DEUTERIUM; FLOWERS; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; MOLECULAR STRUCTURE; MONOTERPENES; STEREOISOMERISM;

ACTINIDIA ARGUTA; ACTINIDIA DELICIOSA;

EID: 34250770459     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2007.03.023     Document Type: Article

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