Synthesis of 3-5-diacyl-4-phenyl-1,4-dihydropyridines

DOI: 10.1016/S0040-4039(98)02084-X

Source and publish data:

Tetrahedron Letters p. 9275 - 9278 (1998)

Update date:2022-08-04

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Authors:

Bennasar, M.-Lluisa

Juan, Cecilia

Bosch, Joan

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Article abstract of DOI:10.1016/S0040-4039(98)02084-X

3,5-Diacyl-4-phenyl-1,4-dihydropyridines have been synthesized via a regio- and chemoselective addition of Ph₂Cu(CN)Li₂ to β-substituted N- alkylpyridinium salts, followed by acylation of the intermediate 1,4- dihydropyridines with t

Full text of DOI:10.1016/S0040-4039(98)02084-X

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Product name:1-Methyl-4-phenyl-5-(2,2,2-trichloro-acetyl)-1,4-dihydro-pyridine-3-carbonitrile

Cas No:219786-72-8

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Article Doi

Synthesis of 3-5-diacyl-4-phenyl-1,4-dihydropyridines

DOI: 10.1016/S0040-4039(98)02084-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(98)02084-X

Full text of DOI:10.1016/S0040-4039(98)02084-X

Products guided by the article

R&D Labs maybe for 219786-72-8

Relevant to this article

Stereoselective sulfoxidation of α-mannopyranosyl thioglycosides: The exo-anomeric effect in action

Short synthesis of piperidine based hexopyranose mimics. A remarkable example of syn hydrogenation

Syntheses, Structures, and Reactivity of Dinuclear Molybdenum-Platinum and Tungsten-Platinum Complexes with Bridging Carbonyl, Sulfur Dioxide, Isonitrile, and Aminocarbyne Ligands and a dppa Backbone (dppa = Ph2PNHPPh2)

One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl- protected amines from ketones

Synthesis of enantiopure 2-aminoalkylphenols by stereoselective addition of Grignard reagents to chiral 2-imidoylphenols

IOOC route to substituted chiral pyrrolidines. Potential glycosidase inhibitors

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