181704-70-1Relevant articles and documents
One pot synthesis of substituted dihydroindeno[1,2-b]indoles and dihydrobenzo[a]carbazoles by photostimulated reactions of o-iodoaniline with carbanions by the SRN1 mechanism
Barolo, Silvia M.,Rosales, Cecire,Angel Guio, Jorge E.,Rossi, Roberto A.
, p. 695 - 699 (2007/10/03)
The photostimulated reaction of enolate anions of cyclic aromatic ketones such as substituted indan-1-ones and 3,4-dihydro-2H-naphthalen-1-one with o-iodoaniline in DMSO affords 1-, 2-, 3-, and 4-methoxy-5,10-dihydroindeno[1,2- b]indoles (34-40%), 1,2-, 1,4-, and 2,3-dimethoxy-5,10-dihydroindeno[1,2-b]- indoles (31-43%), and 1-, 2-, and 3-methoxy-5,11-dihydro-6H-benzo[a]carbazoles (42-61%) by the SRN1 mechanism in one pot reactions.