119128-13-1Relevant articles and documents
Iron(III) chloride-catalyzed convenient one-pot synthesis of β-acetamido carbonyl compounds
Khan, Abu T.,Parvin, Tasneem,Choudhury, Lokman H.
, p. 5593 - 5601 (2007/12/25)
A one-pot multi-component reaction of aldehydes, enolizable ketones or 1,3-dicarbonyls, acetonitrile/benzonitrile, and acetyl chloride is described for the preparation of β-acetamido carbonyl compounds using FeCl3·6H2O as a mild, inexpensive, and highly efficient catalyst. The effect of substrate as well as substituent for multi-component reaction versus Knoevenagel condensation is also illustrated. The key features of this methodology are operational simplicity, mild reaction conditions, and good yields.
Calcium entry blockers and activators: Conformational and structural determinants of dihydropyrimidine calcium channel modulators
Rovnyak,Kimball,Beyer,Cucinotta,DiMarco,Gougoutas,Hedberg,Malley,McCarthy,Zhang,Moreland
, p. 119 - 129 (2007/10/02)
Dihydropyrimidines 4, 6, and 15, uniquely designed to unambiguously establish structural and conformational determinants for DHP receptor occupation and for modulation of calcium channel function, were prepared and examined for calcium channel modulation.
Nitroketeneaminals, VI: Synthesis of methyl 4-aryl-1,4-dihydro- and 4-aryl-4,5-dihydro-5-nitro-nicotinates
Troschutz,Luckel
, p. 73 - 77 (2007/10/02)
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