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Volumn , Issue 16, 2010, Pages 2767-2770
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An efficient synthesis of fused 3-formylpyridines and 5-formylpyrimidines
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Author keywords
2 dimethylaminomethylene 1,3 bis(dimethylimonio)propane diperchlorate; amino heterocycles; cyclization reactions; fused pyridines; fused pyrimidines
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Indexed keywords
CYCLIZATION REACTIONS;
EFFICIENT SYNTHESIS;
FUSED PYRIMIDINE;
FUSED PYRIMIDINES;
HETEROCYCLES;
HETEROCYCLIC SYSTEMS;
AROMATIC COMPOUNDS;
PROPANE;
PYRIDINE;
CYCLIZATION;
1 (1,1 DIOXIDOTETRAHYDRO 3 THIENYL) 3 METHYL 1H PYRAZOLO[3,4 B]PYRIDINE 5 CARBALDEHYDE;
1 (1,1 DIOXIDOTETRAHYDRO 3 THIENYL) 3 METHYL 1H PYRAZOLO[3,4 B]PYRIMIDINE 5 CARBALDEHYDE;
1 TERT BUTYL 5 FORMYL 1H PYRROLO[2,3 B]PYRIDINE 3 CARBONITRILE;
1,3 DIMETHYL 1H PYRAZOLO[3,4 B]PYRIDINE 5 CARBALDEHYDE;
2 DIMETHYLAMINOMETHYLENE 1,3 BIS(DIMETHYLIMONIO)PROPANE DIPERCHLORATE;
2 METHYLPYRAZOLO[1,5 A]PYRIMIDINE 6 CARBALDEHYDE;
2 PHENYL[1,2,4]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBALDEHYDE;
3 (4 METHYLPHENYL)ISOXAZOLO[5,4 B]PYRIDINE 5 CARBALDEHYDE;
3 FORMYLPYRIDINE DERIVATIVE;
3 ISOPROPYLISOXAZOLO[5,4 B]PYRIDINE 5 CARBALDEHYDE;
3 METHYL 1H PYRAZOLO[3,4 B]PYRIDINE 5 CARBALDEHYDE;
3 METHYL 1H PYRAZOLO[3,4 B]PYRIMIDINE 5 CARBALDEHYDE;
3 METHYLISOXAZOLO[5,4 B]PYRIDINE 5 CARBALDEHYDE;
3 TERT BUYLISOXAZOLO[5,4 B]PYRIDINE 5 CARBALDEHYDE;
5 FORMYLPYRIMIDINE DERIVATIVE;
6 FORMYLPYRAZOLO[1,5 A]PYRIMIDINE 3 CARBONITRILE;
ETHYL 6 FORMYLPYRAZOLO[1,5 A]PYRIMIDINE 3 CARBOXYLIC ACID;
HETEROCYCLIC AMINE;
METHYL 5 FORMYL 3 METHYLTHIENO[2,3 B]PYRIDINE 2 CARBOXYLIC ACID;
METHYL 5 FORMYLFURO[2,3 B]PYRIDINE 2 CARBOXYLIC ACID;
METHYL 5 FORMYLTHIENO[2,3 B]PYRIDINE 2 CARBOXYLIC ACID;
METHYL 6 FORMYLTHIENO[2,3 B]PYRIDINE 2 CARBOXYLIC ACID;
PERCHLORATE;
PYRIDINE DERIVATIVE;
PYRIMIDINE DERIVATIVE;
PYRIMIDO[1,2 A]BENZIMIDAZOLE 3 CARBALDEHYDE;
UNCLASSIFIED DRUG;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
LIQUID CHROMATOGRAPHY;
MASS SPECTROMETRY;
PROTON NUCLEAR MAGNETIC RESONANCE;
SYNTHESIS;
THIN LAYER CHROMATOGRAPHY;
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EID: 77955368196
PISSN: 00397881
EISSN: 1437210X
Source Type: Journal
DOI: 10.1055/s-0030-1258139 Document Type: Article |
Times cited : (10)
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References (17)
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