1980
DOI: 10.1021/cr60326a004
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Properties and reactions of ylidenemalononitriles

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Cited by 308 publications
(153 citation statements)
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“…These CHC derivatives of α-cyanocinnamic acids were synthesized from corresponding aldehydes via Knoevenagel type condensation (1−9, Scheme 1B). 20 The compounds 1−9 were evaluated for their MCT1 inhibition activity via [ 14 C]-lactate uptake assay on rat brain endothelial 4 cells (RBE4). We utilized this cell line for initial lactic acid transport studies as they highly express MCT1 as confirmed by Western blotting.…”
mentioning
confidence: 99%
“…These CHC derivatives of α-cyanocinnamic acids were synthesized from corresponding aldehydes via Knoevenagel type condensation (1−9, Scheme 1B). 20 The compounds 1−9 were evaluated for their MCT1 inhibition activity via [ 14 C]-lactate uptake assay on rat brain endothelial 4 cells (RBE4). We utilized this cell line for initial lactic acid transport studies as they highly express MCT1 as confirmed by Western blotting.…”
mentioning
confidence: 99%
“…Knoevenagel condensation is one of the most important methodologies for carbon-carbon double bond formation in synthetic chemistry (Freeman, 1980;Tietze, 1996). The condensation products are the key intermediates for synthesis of natural and therapeutic drugs, polymer, cosmetics and perfumes (Tietze, 2004;Yu et al, 2000).…”
Section: Condensation Under Solvent-free Conditionsmentioning
confidence: 99%
“…2 Knoevenagel condensation have numerous applications in the elegant synthesis of fine chemicals, 3 hetero Diels-Alder reactions 4 and in the synthesis of carbocyclic as well as heterocyclic 5 compounds of biological significance. The products of Knoevenagel condensation have found increasing applications in industry, agriculture, medicine and biological science.…”
Section: Knoevenagel Condensationmentioning
confidence: 99%
“…The products of Knoevenagel condensation have found increasing applications in industry, agriculture, medicine and biological science. 3,6 Substituted cinnamic acids possess a wide range of activities such as antiallergic 7 and in the synthesis of substituted styrenes. 8 Numerous reagents have been reported for Knoevenagel condensation in literature such as triethylbenzylammonium chloride (TEBA), 9 NaCl and NH4 OAc-AcOH, 10 26 anionexchange resin, 27 12-tungstophophoric acid.…”
Section: Knoevenagel Condensationmentioning
confidence: 99%