Oxa-[3+3] annulation of 1H-benzo[f]chromene-2-carbaldehydes and 2-naphthols: synthesis of 7aH,15H-benzo[f]benzo[5,6]chromeno[2,3-b]chromenes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2021-06-26

AUTHORS

Irina А. Semenova, Vitaly А. Osyanin, Dmitry V. Osipov, Yuri N. Klimochkin

ABSTRACT

A method for the preparation of polycondensed chromeno[2,3-b]chromenes was developed based on the formal [3+3] cycloaddition reaction between 1H-benzo[f]chromene-2-carbaldehydes and 2-naphthols. In the case of resorcinol, the bisannulation product formed with the participation of both hydroxy groups was isolated.

PAGES

691-694

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-021-02968-6

DOI

http://dx.doi.org/10.1007/s10593-021-02968-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1139176497


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