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Through‐Bond/Through‐Space Anion Relay Chemistry Exploiting Vinylepoxides as Bifunctional Linchpins
Authors:Dr. Ming Z. Chen  Dr. Osvaldo Gutierrez  Dr. Amos B. Smith III
Affiliation:Department of Chemistry, University of Pennsylvania, 231 S. 34thStreet, Philadelphia, PA 19104 (USA)
Abstract:The development of new bifunctional linchpins that permit the union of diverse building blocks is essential for the synthetic utility of anion relay chemistry (ARC). The design, synthesis, and validation of three vinylepoxide linchpins for through‐bond/through‐space ARC are now reported. For negative charge migration, this class of bifunctional linchpins employs initial through‐bond ARC by an SN2′ reaction, followed by through‐space ARC exploiting a 1,4‐Brook rearrangement. The trans‐disubstituted vinylepoxide linchpin yields a mixture of E/Z isomers, whereas the cis‐disubstituted and the trans‐trisubstituted vinylepoxide linchpins proceed to deliver three‐component adducts with excellent E selectivity.
Keywords:anion relay chemistry  Brook rearrangement  nucleophilic addition  through‐bond interactions  through‐space interactions
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