93973-60-5Relevant articles and documents
Cobalt-Catalyzed Diastereoselective [4+2] Annulation of Phosphinamides with Heterobicyclic Alkenes at Room Temperature
Nallagonda, Rajender,Thrimurtulu, Neetipalli,Volla, Chandra M. R.
supporting information, p. 255 - 260 (2017/11/13)
Cobalt-catalyzed sp2 C?H bond functionalization of diarylphosphinamides with heterobicyclic alkenes was demonstrated at room temperature employing commercially available cobalt(II)-salts. The effectiveness of this strategy was illustrated with the reaction of various 8-aminoquinoline derived phosphinic amides and 7-oxa/azabenzonorbornadienes. The reaction conditions exhibited excellent functional group tolerance and high diastereoselectivities. Furthermore, extension of this approach to the preparation of polyaryl cyclic phosphinamides was achieved through the dehydrative ring opening/aromatization sequence. (Figure presented.).