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Easy Access to Pyranoacridines, Pyranoxanthenes, and Arylchromenes Through a Domino Reaction
Author(s) -
Commandeur Claude,
Florent JeanClaude,
Rousselle Patricia,
Bertounesque Emmanuel
Publication year - 2011
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201001598
Subject(s) - chemistry , domino , benzophenone , xanthone , reagent , combinatorial chemistry , cascade reaction , organic chemistry , catalysis
Abstract A series of pyrano[2,3,4‐ kl ]acridines has been synthesized through an unprecedented domino reaction involving1‐hydroxy‐3‐methoxy‐10‐methylacridone and Grignard reagents. This method has been successfully applied to xanthone, anthracenone, and benzophenone derivatives, thus providing novel access to pyranoxanthenes, dihydronaphthochromenes, and arylchromenes.