Stereoselective synthesis of cyclobutanes by contraction of pyrrolidines

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Abstract

Here we report a contractive synthesis of multisubstituted cyclobutanes containing multiple stereocenters from readily accessible pyrrolidines using iodonitrene chemistry. Mediated by a nitrogen extrusion process, the stereospecific synthesis of cyclobutanes involves a radical pathway. Unprecedented unsymmetrical spirocyclobutanes were prepared successfully, and a concise, formal synthesis of the cytotoxic natural product piperarborenine B is reported.

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APA

Hui, C., Brieger, L., Strohmann, C., & Antonchick, A. P. (2021). Stereoselective synthesis of cyclobutanes by contraction of pyrrolidines. Journal of the American Chemical Society, 143(45), 18864–18870. https://doi.org/10.1021/jacs.1c10175

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