1997
DOI: 10.1055/s-1997-1354
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A Convenient and Regioselective Synthesis of 4-Trifluoromethylpyridines

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Cited by 51 publications
(26 citation statements)
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“…127 The reaction of the enone 391 with -aminocrotononitrile results in the formation of 6-trifluoromethyldihydropyridine 392 in a low yield; oxidation of this product leads to the corresponding aromatic derivative 393. 128 …”
Section: Scheme 110mentioning
confidence: 99%
“…127 The reaction of the enone 391 with -aminocrotononitrile results in the formation of 6-trifluoromethyldihydropyridine 392 in a low yield; oxidation of this product leads to the corresponding aromatic derivative 393. 128 …”
Section: Scheme 110mentioning
confidence: 99%
“…A total of five different trifluoromethyl-β-diketones 1 a-e were synthesized as reported 9 and used in this work. The choice of these particular-β-diketones was determined by their synthetic accessibility.…”
Section: Resultsmentioning
confidence: 99%
“…The crystal data of 4c: 4 ) and concentrated in vacuo. The residue was chromatographed over silica gel, eluted with hexane/ethyl acetate (5/1) to give 4a as a sole product.…”
Section: Methodsmentioning
confidence: 99%
“…Thus, trifluoromethyl-substituted compounds are becoming increasingly important for the development of new agrochemicals and medicines. In recent years, the synthesis of fluorinated Oheterocyclic or N-heterocyclic compounds have draw much attention [4][5][6]. The b-ketoesters are well established as synthetic intermediates in heterocyclic chemistry [7].…”
Section: Introductionmentioning
confidence: 99%
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