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Polar effects in free-radical reactions. New selective alkylations of heteroaromatic bases by benzoylperoxide and olefins.
Affiliation:1. National Demonstration Center for Experimental Chemistry Education, Jishou University, Jishou 416000, PR China;2. Key Laboratory of Cluster Science of Ministry of Education, School of Chemistry, Beijing Institute of Technology, Beijing 100081, PR China;3. CQM-Centro de Química da Madeira, Universidade da Madeira, Campus da Penteada, 9000-390 Funchal, Portugal;1. Department of Chemistry, University of Wisconsin−Madison, Madison, WI, United States;2. Discovery Chemistry, Merck & Co., Inc., Kenilworth, NJ, United States;3. Process Chemistry, Merck & Co., Inc., Rahway, NJ, United States;1. Aptuit s.r.l, Via Fleming 4, 37135 Verona, Italy;2. Indivior Inc, The Fairfax Building, 10710 Midlothian Turnpike, Suite 430, Richmond, VA 23235, USA;1. Institute of Chemistry, Saint Petersburg State University, Universitetsky pr. 26, 198504 Saint Petersburg, Russia;2. Neurofarba Department, Universita degli Studi di Firenze, Florence, Italy
Abstract:The decomposition of benzoylperoxide in the presence of cyclohexene and 1-methylcyclohexene and protonated lepidine provides a new type of selective homolytic aromatic substitution.
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