Preparation of New Terpenyl β??D??Glucopyranosides by a Modified Königs??Knorr Procedure
…, DV Banthorpe, WD Fordham, JP Kinder…
Index: Ackermann, Irmtraud E.; Banthorpe, Derek V.; Fordham, William D.; Kinder, John P.; Poots, Ian Liebigs Annalen der Chemie, 1989 , p. 79 - 82
Full Text: HTML
Citation Number: 14
Abstract
Abstract Ten new hemi-and monoterpenyl β-D-glucopyranosides have been prepared by a modification of the Königs-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.
Related Articles:
Novel reaction systems for the synthesis of O-glucosides by enzymatic reverse hydrolysis
[Balogh, Terez; Boross, Laszlo; Kosary, Judit Tetrahedron, 2004 , vol. 60, # 3 p. 679 - 682]
[Matsushita, Yoh-Ichi; Nagatomo, Hidetaka; Sugamoto, Kazuhiro; Matsui, Takanao Letters in Organic Chemistry, 2009 , vol. 6, # 2 p. 115 - 119]
[Hanessian, Stephen; Bacquet, Christian; Lehong, Nghiep Carbohydrate Research, 1980 , vol. 80, p. C17 - C22]
[Hanessian, Stephen; Bacquet, Christian; Lehong, Nghiep Carbohydrate Research, 1980 , vol. 80, p. C17 - C22]
[Hanessian, Stephen; Bacquet, Christian; Lehong, Nghiep Carbohydrate Research, 1980 , vol. 80, p. C17 - C22]