Reactivity of 4‐chlorobenzo[ c ][2,7]naphthyridines towards Pd(0) catalyzed coupling reactions and nucleophilic substitutions. aroylation by nucleophilic substitution with analogues of acyl anions | Zendy

Duvey G. | Zendy; Nivoliers F. | Zendy; Rocca P. | Zendy; Godard A. | Zendy; Marsais F. | Zendy; Quéguiner G. | Zendy

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Reactivity of 4‐chlorobenzo[ c ][2,7]naphthyridines towards Pd(0) catalyzed coupling reactions and nucleophilic substitutions. aroylation by nucleophilic substitution with analogues of acyl anions

Author(s) -

Duvey G.,

Nivoliers F.,

Rocca P.,

Godard A.,

Marsais F.,

Quéguiner G.

Publication year - 2001

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.5570380505

Subject(s) - chemistry , nucleophilic substitution , reactivity (psychology) , nucleophile , medicinal chemistry , iodide , catalysis , substitution reaction , derivative (finance) , stereochemistry , organic chemistry , medicine , alternative medicine , pathology , financial economics , economics

Various 4‐substituted benzo[ c ][2,7]naphthyridines were prepared from the corresponding 4‐chloro derivative by Pd(0) coupling reaction or nucleophilic substitution. More particularly, 4‐aroyl‐benzo[e][2,7]naph‐thyridines were synthesized by aroylation with arenecarbaldehydes in the presence of 1,3‐dimethylimida‐zolium iodide.

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