An efficient route toward 2-amino-β-D-galacto-and -glucopyranosides via stereoselective michael-type addition of 2-nitroglycals

Journal of Organic Chemistry

Volumn 74, Issue 14, 2009, Pages 5079-5082

  Xue, Weihua ^a   Sun, Jiansong ^a   Yu, Biao ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; D-GALACTOSAMINE; GLUCOSAMINE; STEREO-SELECTIVE;

AMINES;

STEREOSELECTIVITY;

2 AMINO BETA GALACTOPYRANOSIDE DERIVATIVE; 2 AMINO BETA GLUCOPYRANOSIDE DERIVATIVE; GALACTOSAMINE; GLUCOPYRANOSIDE; GLUCOSAMINE; NITROGEN DERIVATIVE; NUCLEOPHILE; PYRANOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; MICHAEL ADDITION; PRECURSOR; QUANTUM YIELD; REACTION ANALYSIS; STEREOCHEMISTRY;

CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; GLUCOSIDES; GLYCOSYLATION; MOLECULAR STRUCTURE; PYRANS; STEREOISOMERISM;

EID: 67650351956     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900609s     Document Type: Article

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