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Volumn 58, Issue 1, 2002, Pages 75-82
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An enantioselective formal synthesis of 4-demethoxydaunomycin using the catalytic asymmetric ring opening reaction of meso-epoxide with p-anisidine
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Author keywords
4 demethoxydaunomycin; Catalytic asymmetric ring opening reaction; Multifunctional catalyst
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Indexed keywords
4 DEMETHOXYDOXORUBICIN;
5,8 DIMETHOXY 3 (4 METHOXYPHENYLAMINO) 1,2,3,4 TETRAHYDRONAPHTHALEN 2 OL;
[1 (1,1 ETHYLENEDIOXY)ETHYL] 1,2,3,4 TETRAHYDRO 5,8 DIMETHOXYNAPHTHALENE 1,3 DIYLBENZENEBORONATE;
AMINOALCOHOL;
DAUNORUBICIN;
DOXORUBICIN;
EPOXIDE;
IDARUBICIN;
PARA ANISIDINE;
UNCLASSIFIED DRUG;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CATALYSIS;
CATALYST;
COLUMN CHROMATOGRAPHY;
CRYSTALLIZATION;
DRUG SYNTHESIS;
ENANTIOMER;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
METHYLATION;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEREOCHEMISTRY;
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EID: 0036135096
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)01088-2 Document Type: Article |
Times cited : (100)
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References (46)
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