Synthesen in der Reihe der Tosyl‐zucker
Author:
Affiliation:
1. Kaiser‐Wilhelm‐Institut für Chemie, Berlin‐Dahlem
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19340670405
Reference38 articles.
1. Tri-tosylstärke, Di-tosyl-6-jodstärke und Tri-benzoylstärke. 4. Mitteilung über Stärke
2. Über den Abbau von Tri-tosylstärke und Di-tosyl-6-jodstärke mit Bromwasserstoff–Eisessig. 5. Mitteilung über Stärke
3. Tosyl =p‐Toluol‐sulfonyl.
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1. Synthesis of an artificial antigen that corresponds to a disaccharide repeating unit of the capsular polysaccharide of Haemophilus influenzae type d. A facile synthesis of methyl 2-acetamido-2-deoxy-β- d -mannopyranoside;Carbohydrate Research;1992-09
2. Desulfonyloxylations of some secondary p-toluenesulfonates of glycosides by lithium triethylborohydride; a high-yielding route to 2- and 3-deoxy sugars;Carbohydrate Research;1982-11
3. Spectrométrie de Masse de Benzylidène—Acétals d'Hexopyranosides;Organic Mass Spectrometry;1977-08
4. Specific spectral assignments for acetoxyl-group resonances in proton magnetic resonance spectra of methyl β-D-glucopyranoside tetraacetate and related derivatives;Carbohydrate Research;1975-08
5. Hydrazinolysis of Sugar Sulfonates;Bulletin of the Chemical Society of Japan;1970-09
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