A new method for the stereoselective synthesis of α- and β-glycosylamines using the Burgess reagent

Journal of the American Chemical Society

Volumn 126, Issue 20, 2004, Pages 6234-6235

  Nicolaou, K C ^a   Snyder, Scott A ^a   Nalbandian, Annie Z ^a   Longbottom, Deborah A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLYCOSYLAMINE; AMINE; BETA GLYCOSYLAMINE; CARBOHYDRATE; GLUCOSE; REAGENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

AMINO SUGARS; CARBOHYDRATES; CRYSTALLOGRAPHY, X-RAY; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM;

EID: 2442671540     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja049293c     Document Type: Article

References (16)

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12. It is important to note that this protocol does not provide a general synthesis of aminals from lactols, as a number of conventional lactols gave inconsistent yields of the desired products.
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14. The only incompatibility that we have identified is the presence of carbonyl-based protecting groups such as acetate or benzoate at the C-3 position.
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