Neighboring-group participation in benzylidene acetal ring-opening of a 2-cyano-2-deoxypyranoside derivative by diethylaluminum cyanide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference30 articles.
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2. Recent advances in the stereoselective synthesis of carbohydrate 2-C-analogs;Organic & Biomolecular Chemistry;2012
3. Some observations on the reductive ring opening of 4,6-O-benzylidene acetals of hexopyranosides with the borane trimethylamine–aluminium chloride reagent;Carbohydrate Research;2011-09
4. Cyanodeoxy-Glycosyl Derivatives as Substrates for Enzymatic Reactions;European Journal of Organic Chemistry;2006-04
5. Synthesis of methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-formyl-α-d-erythro-hex-2-enopyranoside;Carbohydrate Research;2005-01
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