The Separation and purification of ribofuranose derivates by countercurrent distribution
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19740830308/fullpdf
Reference9 articles.
1. Steady State Distribution
2. Evidence that the Supposed 3,5-Di-O-benzoyl-1,2-O-(1-hydroxybenzylidene)-α-D- ribose is Actually 1,3,5-Tri-O-benzoyl-α-D-ribose
3. Eine neue, einfache Synthese des. 1-O-Acetyl-2,3,5-Tri-O-benzoyl-?-D-Ribofuranosides
4. Synthese von β‐Ribazol ausgehend von Adenosin
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1. 1,2-Orthoester Formation and Glycosidation with Amide Acetals;General Methods;1980
2. Nucleoside, XXIX. Über die Synthese des 6,7‐Diphenyl‐3‐(β‐ D ‐ribofuranosyl)lumazins auf direktem Wege und mit Hilfe einer photolabilen N ‐8‐Schutzgruppe;Chemische Berichte;1978-07
3. Chemistry of the glycosidic linkage.O-glycosylations catalyzed by stannic chloride, in the D-ribofuranose and D-glucopyranose series;Carbohydrate Research;1977-11
4. Chemistry of the glycosidic linkage. Lewis acid catalyzed glycosidations with amide acetals and lactim ethers.;Tetrahedron Letters;1976-02
5. ChemInform Abstract: THE SEPARATION AND PURIFICATION OF RIBOFURANOSE DERIVATIVES BY COUNTERCURRENT DISTRIBUTION;Chemischer Informationsdienst;1974-07-23
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