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Volumn 65, Issue 22, 2000, Pages 7627-7633
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Stereoselective preparation of ceramide and its skeleton backbone modified analogues via cyclic thionocarbonate intermediates derived by catalytic asymmetric dihydroxylation of α,β-unsaturated ester precursors
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Author keywords
[No Author keywords available]
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Indexed keywords
AZIDE;
CARBONIC ACID;
CERAMIDE;
ESTER;
OSMIUM;
SPHINGOLIPID;
SPHINGOSINE;
THIOCARBONATE DERIVATIVE;
UNCLASSIFIED DRUG;
ACYLATION;
ARTICLE;
CATALYSIS;
CHEMICAL MODIFICATION;
CHIRALITY;
ENANTIOMER;
HYDROXYLATION;
STEREOCHEMISTRY;
STEREOISOMERISM;
SYNTHESIS;
CATALYSIS;
CERAMIDES;
ESTERS;
HYDROXYLATION;
INDICATORS AND REAGENTS;
SPHINGOSINE;
STEREOISOMERISM;
SULFIDES;
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EID: 0034602328
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo001226n Document Type: Article |
Times cited : (51)
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References (53)
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