A short procedure for the preparation of highly functionalized di- and tetrahydropyridines

DOI: 10.1016/S0040-4039(99)00621-8

Source and publish data:

Tetrahedron Letters p. 3961 - 3964 (1999)

Update date:2022-08-05

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Authors:

Bennasar, M. -Lluisa

Zulaica, Ester

Juan, Cecilia

Llauger, Laura

Bosch, Joan

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Article abstract of DOI:10.1016/S0040-4039(99)00621-8

The addition of a series of stabilized carbon nucleophiles to 3-acyl-1- alkylpyridinium salts, followed by acylation of the intermediate dihydropyridines with trichloroacetic anhydride has been studied. The C-4 adducts resulting from the addition of α-(me

Full text of DOI:10.1016/S0040-4039(99)00621-8

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