916595-90-9Relevant academic research and scientific papers
Synthesis of certain monoterpenoid glucosides
Patov,Punegov,Kuchin,Frolova
, p. 431 - 433 (2006)
The monoterpenols borneol, verbenol, 4-(1-hydroxyethyl)carene-2, and myrtenol were glucosylated using acetobromoglucose. The structures of the prepared derivatives were established using PMR and 13C NMR spectroscopy.
Preparation of New Terpenyl β-D-Glucopyranosides by a Modified Koenigs-Knorr Procedure.
Ackermann, Irmtraud E.,Banthorpe, Derek V.,Fordham, William D.,Kinder, John P.,Poots, Ian
, p. 79 - 82 (2007/10/02)
Ten new hemi- and monoterpenyl β-D-glucopyranosides have been prepared by a modification of the Koenigs-Knorr procedure which utilises silver fluoroacetate as a soluble catalyst coupled with the introduction of a basic ion-exchange resin to effect the deacetylation step.Most of these compounds could not be obtained in acceptable yields using the classical procedure.
