Benutzer-Werkzeuge

Webseiten-Werkzeuge


passiflora_edulis

Unterschiede

Hier werden die Unterschiede zwischen zwei Versionen angezeigt.

Link zu dieser Vergleichsansicht

Beide Seiten der vorigen Revision Vorhergehende Überarbeitung
Nächste Überarbeitung
Vorhergehende Überarbeitung
Nächste Überarbeitung Beide Seiten der Revision
passiflora_edulis [2017/06/22 09:49]
andreas
passiflora_edulis [2020/06/23 09:36]
andreas
Zeile 8: Zeile 8:
 3-Methylthio-hexanol as well as (Z) and (E)-2-methyl-4-propyl-1,3-oxathiane were identified as character impact compounds in a flavor concentrate of the yellow passion fruit of Hawaiian origin. \\ 3-Methylthio-hexanol as well as (Z) and (E)-2-methyl-4-propyl-1,3-oxathiane were identified as character impact compounds in a flavor concentrate of the yellow passion fruit of Hawaiian origin. \\
 [Identification and synthesis of two new organic sulfur compounds from the yellow passion fruit (Passiflora edulis f. flavicarpa)., Winter, M., Furrer, A., Willhalm, B., Thommen, W., Helvetica Chimica Acta, 59(5), 1976, 1613-1620] [Identification and synthesis of two new organic sulfur compounds from the yellow passion fruit (Passiflora edulis f. flavicarpa)., Winter, M., Furrer, A., Willhalm, B., Thommen, W., Helvetica Chimica Acta, 59(5), 1976, 1613-1620]
 +
 +The strikingly fresh-fruity ethyl (Z)‐4,7‐octadienoate and (Z)‐3,5‐hexadienyl butyrate are important aroma constituents of the purple passionfruit. \\
 +[Winter, Max, et al. "(Z)‐4,7‐Octadiensäure‐äthylester und (Z)‐Buttersäure‐3,5‐hexadienylester, zwei neue Aromastoffe der roten Passionsfrucht." Helvetica Chimica Acta 62.1 (1979): 135-139]
  
 Enantioselective synthesis starting form (E)-2-hexenol showed that (+)- and (-)-(Z)-2-methyl-4-propyl-1,3-oxathiane exhibit different organoleptic properties. Whereas the (+)-enantiomer had a estery-camphoraceous-flowery type odor, (-)-(Z)-2-methyl-4-propyl-1,3-oxathiane smelled powerful sulfury, tropical-fruit-like (th 4ppm). \\ Enantioselective synthesis starting form (E)-2-hexenol showed that (+)- and (-)-(Z)-2-methyl-4-propyl-1,3-oxathiane exhibit different organoleptic properties. Whereas the (+)-enantiomer had a estery-camphoraceous-flowery type odor, (-)-(Z)-2-methyl-4-propyl-1,3-oxathiane smelled powerful sulfury, tropical-fruit-like (th 4ppm). \\
 [Enantioselective synthesis of (+)‐and (-)‐cis‐2‐methyl‐4‐propyl‐1,3‐oxathiane and their olfactive properties., Pickenhagen, W., Brönner‐Schindler, H., Helvetica chimica acta, 67(4), 1984, 947-952] [Enantioselective synthesis of (+)‐and (-)‐cis‐2‐methyl‐4‐propyl‐1,3‐oxathiane and their olfactive properties., Pickenhagen, W., Brönner‐Schindler, H., Helvetica chimica acta, 67(4), 1984, 947-952]
  
-|{{:oxane.jpg}} \\ (-)-(Z)-2-methyl-4-propyl-1,3-oxathiane \\ //(sulfury, tropical fruit)// |{{:3methylthiohexyl_deriv.jpg}} \\ 3-(methylthio)hexanol (R=H) and esters (R=Ac, ...) \\ //(sulfury, green fruity)// |+|{{:oxane.jpg}} \\ (-)-(Z)-2-methyl-4-propyl-1,3-oxathiane \\ //(sulfury, tropical fruit)// |{{:3mercaptohexanol.png}} \\ 3-mercaptohexanol \\ //(grapefruit, tropical fruit, fresh)// |{{:3methylthiohexyl_deriv.jpg}} \\ 3-(methylthio)hexanol (R=H) and esters (R=Ac, ...) \\ //(sulfury, green fruity)// |
  
  
passiflora_edulis.txt · Zuletzt geändert: 2021/03/11 10:36 von andreas