Displacement of “pseudoanomeric” hydroxyl groups by using the diethyl azodicarboxylate-triphenylphosphine system
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
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2. Synthesis of amylostatin (XG), α-glucosidase inhibitor with basic pseudotrisaccharide structure
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4. Cyclit-Reaktionen, V. Synthese von enantiomerenreinem Valienamin aus Quebrachit
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1. Synthesis and α-Glucosidase II inhibitory activity of valienamine pseudodisaccharides relevant to N-glycan biosynthesis;Bioorganic & Medicinal Chemistry Letters;2011-09
2. Investigation of Coupling Reactions for the Synthesis of Valienamine Pseudodisaccharides;Synlett;2011-06-21
3. Studies on the synthesis of valienamine and 1-epi-valienamine starting from d-glucose or l-sorbose;Carbohydrate Research;2008-07
4. Formal synthesis of valienamine using ring-closing metathesis;Tetrahedron Letters;2005-09
5. β-Acarbose. I The Synthesis of 1-Epivalienamine;Australian Journal of Chemistry;1997
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