Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 9, Issue 10, Pages 3929-3939Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob05068k
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- Nanyang Technological University [RG50/08]
- Ministry of Education, Singapore [MOE 2009-T2-1-030]
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A highly stereoselective BF3 center dot OEt2-promoted tandem hydroamination-glycosylation on a glycal scaffold has been developed to form 3-amino-2,3-dideoxysugars in a one-pot procedure. This efficient multicomponent reaction protocol offers simplicity and general applicability to a broad range of variations on each component.
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