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Journal of Organic Chemistry

Volumn 75, Issue 10, 2010, Pages 3443-3446

Synthesis of all configurational isomers of 1,6-anhydro-2,3,4-trideoxy-2,3- epimino-4-fluoro-β- d -hexopyranoses

(6) Karban, Jindřich a Sýkora, Jan a Kroutil, Jiří b Císařová, Ivana b Padělková, Zdeňka c Buděšínský, Miloš d

a INSTITUTE OF CHEMICAL PROCESS FUNDAMENTALS (Czech Republic)

b CHARLES UNIVERSITY (Czech Republic)

c UNIVERSITY OF PARDUBICE (Czech Republic)

d INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

CONFIGURATIONAL ISOMERS; GOOD YIELD; NUCLEOPHILIC DISPLACEMENT;

ISOMERS;

SYNTHESIS (CHEMICAL);

1,6 ANHYDRO 2,3,4 TRIDEOXY 2,3 EPIMINO 4 FLUORO BETA DEXTRO HEXOPYRANOSE; DIETHYLAMINOSULFUR TRIFLUORIDE; FLUORIDE; HYDROXYL GROUP; NUCLEOPHILE; PYRAN DERIVATIVE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; ISOMER; REDUCTION KINETICS; SYNTHESIS;

AZIDES; CARBOHYDRATES; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 77952509133 PISSN: 00223263 EISSN: 15206904 Source Type: Journal
DOI: 10.1021/jo1000912 Document Type: Article

Times cited : (19)

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