Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-4,4-difluoronojirimycin

Organic Letters

Volumn 7, Issue 11, 2005, Pages 2189-2192

  Wang, Ruo Wen ^a   Qing, Feng Ling ^a,b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b DONGHUA UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE DERIVATIVE; DEXTRO 1,4,6 TRIDEOXY 4,4 DIFLUORONOJIRIMYCIN; LEVO 1,4,6 TRIDEOXY 4,4 DIFLUORONOJIRIMYCIN; PIPERIDINE; UNCLASSIFIED DRUG;

AMINATION; ARTICLE; METHYLATION; STEREOCHEMISTRY; SYNTHESIS;

CATALYSIS; CRYSTALLOGRAPHY, X-RAY; IMINO PYRANOSES; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 20444484514     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol050558h     Document Type: Article

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43. When 9 was subject to the standart conditions of transesterification- based enzymatic resolution and kinetic epoxidation resolution, no reaction was observed.