Details van artikel 143 van 252 gevonden artikelen
Stereoselective Synthiesis of Both Enantiomers of Disparlure from D-Glucose
Titel:
Stereoselective Synthiesis of Both Enantiomers of Disparlure from D-Glucose
Auteur:
Achmatowicz, Osman Sadownik, Andrzej
Verschenen in:
Journal of carbohydrate chemistry
Paginering:
Jaargang 4 (1985) nr. 3 pagina's 435-440
Jaar:
1985-09-01
Inhoud:
D-Glucose was transformed stereoselectively into (7R,8S)8-benzyloxy-7-hydroxy-2-methyl-9-octadecene from which both enantiomers of disparlure, (7R,8S)-(+)-and (7S,8R)-(-)-7,8-epoxy-2-methyloctadecane, sex pheromone of the gypsy moth, were obtained in four and three steps, respectively.
Uitgever:
Taylor & Francis
Bronbestand:
Elektronische Wetenschappelijke Tijdschriften
Details van artikel 143 van 252 gevonden artikelen