125782-83-4Relevant articles and documents
Allene/haloolefin electrocyclic reactions: A new route to stable triarylmethyl radicals
Porter, Ned A.,Hogenkamp, Derk J.,Khouri, Farid F.
, p. 2402 - 2407 (2007/10/02)
Electrocyclization of allene 1,1-diphenyl-3-[2-(2-bromoethenyl)phenyl]propadiene (5), followed by one-electron reduction with elemental mercury, gives β-naphthyldiphenylmethyl radical 6 in good yield. In the absence of mercury, the only product isolated i