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Volumn , Issue 8, 2003, Pages 1559-1568
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Recommendable routes to trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids
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Author keywords
Building blocks; Carboxylation; Heterocycles; Organometallic intermediates; Sulfur tetrafluoride; Trifluoromethylcopper
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Indexed keywords
2 TRIFLUOROMETHYL 3 PYRIDINECARBOXYLIC ACID;
2 TRIFLUOROMETHYL 3 QUINOLINECARBOXYLIC ACID;
2 TRIFLUOROMETHYL 4 PYRIDINECARBOXYLIC ACID;
2 TRIFLUOROMETHYL 4 QUINOLINECARBOXYLIC ACID;
2 TRIFLUOROMETHYL 8 QUINOLINECARBOXYLIC ACID;
3 TRIFLUOROMETHYL 2 PYRIDINECARBOXYLIC ACID;
3 TRIFLUOROMETHYL 2 QUINOLINECARBOXYLIC ACID;
3 TRIFLUOROMETHYL 4 PYRIDINECARBOXYLIC ACID;
3 TRIFLUOROMETHYL 4 QUINOLINECARBOXYLIC ACID;
3 TRIFLUOROMETHYL 8 QUINOLINECARBOXYLIC ACID;
4 TRIFLUOROMETHYL 2 PYRIDINECARBOXYLIC ACID;
4 TRIFLUOROMETHYL 2 QUINOLINECARBOXYLIC ACID;
4 TRIFLUOROMETHYL 3 PYRIDINECARBOXYLIC ACID;
4 TRIFLUOROMETHYL 3 QUINOLINECARBOXYLIC ACID;
4 TRIFLUOROMETHYL 8 QUINOLINECARBOXYLIC ACID;
5 TRIFLUOROMETHYL 2 PYRIDINECARBOXYLIC ACID;
5 TRIFLUOROMETHYL 3 PYRIDINECARBOXYLIC ACID;
6 TRIFLUOROMETHYL 2 PYRIDINECARBOXYLIC ACID;
6 TRIFLUOROMETHYL 3 PYRIDINECARBOXYLIC ACID;
CARBON DIOXIDE;
CARBOXYLIC ACID DERIVATIVE;
FUNCTIONAL GROUP;
ORGANOLITHIUM COMPOUND;
ORGANOMAGNESIUM COMPOUND;
ORGANOMETALLIC COMPOUND;
SULFUR DERIVATIVE;
SULFUR FLUORIDE;
TRIFLUOROMETHYL COPPER;
UNCLASSIFIED DRUG;
ARTICLE;
FLUORINATION;
REACTION ANALYSIS;
SYNTHESIS;
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EID: 0038031793
PISSN: 1434193X
EISSN: None
Source Type: Journal
DOI: 10.1002/ejoc.200390215 Document Type: Article |
Times cited : (122)
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References (48)
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