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cis-Selective synthesis of 2,5-disubstituted pyrrolidines
Authors:Syed Raziullah Hussaini
Institution:The Department of Chemistry, Dyson Perrins Laboratory, The University of Oxford, South Parks Road, Oxford OX1 3QY, UK
Abstract:A concise approach to cis-2,5-disubstituted pyrrolidines is reported, which relies upon N-tert-butoxycarbonylmethyl substitution in a substrate derived from pyroglutamic acid. The method is especially noteworthy since a significant improvement in the conditions for a key Lawesson’s reaction have been established. Regioselective enolate generation and alkylation permits extension of the C-5 side chain.
Keywords:Pyrrolidines  Thionation  Lawesson&rsquo  s reagent
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