81454-09-3Relevant articles and documents
REDUCTIVE DEAMINATION OF ARYL- AND HETEROARYL-AMINES VIA PYRIDINIUM FLUORIDES
Katritzky, Alan R.,Chermprapai, Amornsri,Bravo, Susana,Patel, Ranjan C.
, p. 3603 - 3607 (2007/10/02)
The corresponding "pseudobase" Δ2-1,5-diketones (8) and (14) afford dihydrochromenylium (9a) and tetrahydroxanthylium monofluorides (15).These convert aryl- and heteroarylamines into dihydroquinolinium (10) and tetrahydroacridinium (16) monofluorides which at 130-250 deg C give the deaminated arenes and heteroarenes (average overall yield 60percent).