32779-51-4Relevant articles and documents
Regioselective C-H bond functionalizations of acridines using organozinc reagents
Hyodo, Isao,Tobisu, Mamoru,Chatani, Naoto
supporting information; scheme or table, p. 308 - 310 (2012/01/05)
Despite the recent advance in C-H bond functionalization chemistry, the C-H bonds in the acridine ring system, which is an important scaffold in medicinal and material science, have met with limited success, due, in part, to the lack of activated C-H bonds adjacent to the ring nitrogen atom. Herein, several protocols that can effect the regioselective arylation and alkylation of acridines at the C-4 and C-9 positions are described.
The Synthesis of Some Sterically Hindered Acridines and a High Pressure Methylation
Acheson, R. Morrin,Birtwistle, David H.,Constable, Edward C.,Tester, Gordon G.,Whitehead, W. F.,Wyatt, Peter B.
, p. 2367 - 2383 (2007/10/02)
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