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Volumn 67, Issue 10, 2002, Pages 3525-3528
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A novel approach to the synthesis of amino-sugars. Routes to selectively protected 3-amino-3-deoxy-aldopentoses based on pyridinium salt photochemistry
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Author keywords
[No Author keywords available]
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Indexed keywords
RING-OPENING REACTIONS;
DERIVATIVES;
ENZYMES;
PHOTOCHEMICAL REACTIONS;
SALTS;
STEREOCHEMISTRY;
SYNTHESIS (CHEMICAL);
SUGARS;
3 AMINO 3 DEOXY ALDOPENTOSE DERIVATIVE;
AMINOGLYCOSIDE DERIVATIVE;
DEXTRO 3 AMINO 3 DEOXYXYLOSE DERIVATIVE;
LEVO 3 AMINO 3 DEOXYARABINOSE DERIVATIVE;
LEVO 3 AMINO 3 DEOXYXYLOSE DERIVATIVE;
N ACETYLNEURAMINIC ACID;
PYRIDINIUM DERIVATIVE;
UNCLASSIFIED DRUG;
AMINOSUGAR;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CYCLIZATION;
ENANTIOMER;
PHOTOCHEMISTRY;
PROTON NUCLEAR MAGNETIC RESONANCE;
REACTION ANALYSIS;
STEREOCHEMISTRY;
SYNTHESIS;
CATALYSIS;
CHEMICAL STRUCTURE;
CHEMISTRY;
METHODOLOGY;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
ORGANIC CHEMISTRY;
STEREOISOMERISM;
AMINO SUGARS;
CATALYSIS;
CHEMISTRY, ORGANIC;
CYCLIZATION;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR STRUCTURE;
PHOTOCHEMISTRY;
PYRIDINIUM COMPOUNDS;
STEREOISOMERISM;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
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EID: 0037123433
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo020038p Document Type: Article |
Times cited : (23)
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References (16)
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