The reaction of 4-aminocoumarin with β-carbonyl-substituted 4Н-chromenes: synthesis of 5H-chromeno[4,3-b]pyridin-5-one derivatives View Full Text


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Article Info

DATE

2019-03

AUTHORS

Dmitriy V. Osipov, Alina A. Artyomenko, Vitaly A. Osyanin, Yuri N. Klimochkin

ABSTRACT

Reactions of 4Н-chromene-3-carbaldehydes and 1Н-benzo[f]chromene-3-carbaldehydes with 4-aminocoumarin were used to obtain a series of pyridocoumarin derivatives containing a 2-hydroxybenzyl or 2-hydroxy-1-naphthyl substituent at the β-position relative to the nitrogen atom. The reaction mechanism includes a Michael reaction, chromane ring opening, and cyclodehydration.

PAGES

261-265

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-019-02451-3

DOI

http://dx.doi.org/10.1007/s10593-019-02451-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1113643663


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