Biosynthesis and enantioselectivity in the production of the lilac compounds in Actinidia arguta flowers

Phytochemistry

Volumn 72, Issue 7, 2011, Pages 579-586

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

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

^b Institute for Clean Growth and Future Mobility   (United Kingdom)

Author keywords

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

Indexed keywords

2 (5 METHYL 5 (OXIRAN 2 YL) TETRAHYDROFURAN 2 YL)PROPAN 1 OL; 2-(5-METHYL-5-(OXIRAN-2-YL)-TETRAHYDROFURAN-2-YL)PROPAN-1-OL; ALDEHYDE; DRUG DERIVATIVE; ETHYLENE OXIDE; FURAN DERIVATIVE; LINALOOL; PROPANOL; TERPENE;

ARTICLE; CHEMISTRY; ENZYME SPECIFICITY; FLOWER; GROWTH, DEVELOPMENT AND AGING; KIWIFRUIT; METABOLISM; STEREOISOMERISM;

ACTINIDIA; ALDEHYDES; ETHYLENE OXIDE; FLOWERS; FURANS; MONOTERPENES; PROPANOLS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

ACTINIDIA ARGUTA; ACTINIDIA DELICIOSA;

EID: 79953267029     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2011.01.035     Document Type: Article

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