Enantioselective, intermolecular [2+2] photocycloaddition reactions of 3-acetoxyquinolone: total synthesis of (−)-pinolinone

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Abstract

The natural product (−)-pinolinone was synthesised via a concise route (six steps, 17% overall yield) from 3-acetoxyquinolone, employing an enantioselective intermolecular [2+2] photocycloaddition as the key step. © 2014 The Royal Society of Chemistry.

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Mayr, F., Wiegand, C., & Bach, T. (2014). Enantioselective, intermolecular [2+2] photocycloaddition reactions of 3-acetoxyquinolone: total synthesis of (−)-pinolinone. Chemical Communications, 50(25), 3353–3355. https://doi.org/10.1039/c3cc49469a

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