Reaction of Trimethylsilyl Azide with Anhydro Sugars, a Mild Method of Oxirane-Ring Opening
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Reference11 articles.
1. Advances in Carbohydrate Chemistry and Biochemistry, Vol. 25, p. 109, Acedemic Press, New York 1970.
2. Synthetic Routes to Aminosugars. Efficient One-pot Synthesis of some New Diazidodideoxysugars
3. in Heterocyclic Compounds with Three- and Four-Membered Rings, Part III (Ed.), Interscience, New York 1964.
4. C-4-Triflat-Substitution durch Azid bei 2,3-Anhydrozuckern; ein neuer Weg zu 4-Amino-4-desoxyzuckern
5. Addition von (Trimethylsilyl)azid an Aldehyde und Epoxide1)
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4. Aldonolactones as chiral synthons;Glycoscience Synthesis of Substrate Analogs and Mimetics;1997
5. Highly regio and chemoselective ring opening of epoxides with trimethylsilyl azide in the presence of aluminium isopropoxide and titanium isopropoxide;Tetrahedron;1991-01
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