Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9765840 | Journal of Fluorine Chemistry | 2005 | 6 Pages |
Abstract
A convenient method for the synthesis of a novel series of 7-trifluoromethyl-5,6-dihydrobenzo[c]acridines, in 44-82% yields, by intramolecular cyclization reactions of N-aryl-2-trifluoroacetyl-3,4-dihydronaphthylamines using poly-phosphoric acid (PPA), is described on this paper. Naphthylamine derivatives are obtained by an oxygen-nitrogen exchange reaction from 1-methoxy-2-trifluoroacetyl-3,4-dihydronaphthalene with substituted anilines.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Helio G. Bonacorso, Roberta L. Drekener, Isadora R. Rodrigues, Renata P. Vezzosi, Michelle B. Costa, Marcos A.P. Martins, Nilo Zanatta,