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Stereospecific C–H activation as a key step for the asymmetric synthesis of various biologically active cyclopropanes

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Abstract

A rapid and efficient synthesis of hoshinolactam, an enantiopure cyclopropane containing natural product, is described. This strategy is based on stereospecific C(sp3)–H activation via unprecedented olefination on the cyclopropane core. The use of a stereogenic and easily recyclable directing group (S)-2-(p-tolylsulfinyl)aniline (APS) which was originally developed by our group allows obtention of diastereomerically pure products in high yields. Optically pure cyclopropanes are subsequently converted into enantiomerically pure targeted natural products. Furthermore a closely related synthetic scenario is employed to build up precursors of grenadamide and cascarillic acid.

Graphical abstract: Stereospecific C–H activation as a key step for the asymmetric synthesis of various biologically active cyclopropanes

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Publication details

The article was received on 18 Aug 2017, accepted on 15 Sep 2017 and first published on 19 Sep 2017


Article type: Research Article
DOI: 10.1039/C7QO00737J
Citation: Org. Chem. Front., 2018, Advance Article
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    Stereospecific C–H activation as a key step for the asymmetric synthesis of various biologically active cyclopropanes

    S. Jerhaoui, P. Poutrel, J.-P. Djukic, J. Wencel-Delord and F. Colobert, Org. Chem. Front., 2018, Advance Article , DOI: 10.1039/C7QO00737J

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