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Volumn 329, Issue 3, 2000, Pages 681-686
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Novel ring transformation of 5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)isoxazole-4-carbaldehyde with 1,2-diaminobenzenes to 3-cyano-1,5-benzodiazepine C-nucleosides
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Author keywords
1,5 benzodiazepine C nucleoside; 3 cyano 1,5 benzodiazepine; C nucleoside; Cyclocondensation; Isoxazole carbaldehyde; Synthesis
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Indexed keywords
1,2 DIAMINOBENZENE DERIVATIVE;
3 CYANO 1,5 BENZODIAZEPINE C NUCLEOSIDE DERIVATIVE;
3 CYANO 8 NITRO 4 (2,3,5 TRI O BENZOYL BETA DEXTRO RIBOFURANOSYL) 1H 1,5 BENZODIAZEPINE;
5 (2,3,5 TRI O BENZOYL BETA DEXTRO RIBOFURASONYL) ISOXAZOLE 4 CARBALDEHYDE;
ALDEHYDE DERIVATIVE;
BENZENE DERIVATIVE;
BENZODIAZEPINE DERIVATIVE;
C NUCLEOSIDE;
CYANOBENZODIAZEPINE DERIVATIVE;
ISOXAZOLE CARBALDEHYDE;
ISOXAZOLE DERIVATIVE;
NUCLEOSIDE DERIVATIVE;
TRIFLUOROACETIC ACID;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL STRUCTURE;
PRIORITY JOURNAL;
REACTION TIME;
STEREOCHEMISTRY;
SYNTHESIS;
TEMPERATURE DEPENDENCE;
ALDEHYDES;
BENZODIAZEPINES;
ISOXAZOLES;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR STRUCTURE;
NUCLEOSIDES;
PHENYLENEDIAMINES;
SCHIFF BASES;
SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT;
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EID: 0034680694
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/S0008-6215(00)00231-7 Document Type: Article |
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Times cited : (6)
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References (5)
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