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One-pot two step synthesis of unsymmetrically substituted indenes from 3,4-diarylbutadiene sulfones
Affiliation:A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 119991 Moscow, Russian Federation
Abstract:A new one-pot two step synthesis of unsymmetrically substituted indenes from available 3,4-diarylbutadiene sulfones involves SO2 thermal extrusion followed by acid- catalyzed cyclization of the diene formed, the cyclization proceeding selectively at the more electron-rich aryl rings. The procedure is efficient for substrates bearing donor, acceptor, as well as bulky substituents.
Keywords:indenes  34-diarylbutadienes  sulfones  sulfur dioxide  thermal extrusion  catalytic cyclization  Friedel–Crafts reaction  one-pot synthesis
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