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Rapid, enantioselective synthesis of the C1–C13 fragment of biselyngbyolide B

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Abstract

A rapid synthesis of the C1–C13 fragment of biselynbyolide A and B is reported. The judicious use of catalytic transformations for C–C bond formation and stereocenter generation greatly minimizes the use of protecting groups and oxidation state changes, as compared to previously reported routes to similar fragments.

Graphical abstract: Rapid, enantioselective synthesis of the C1–C13 fragment of biselyngbyolide B

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Publication details

The article was received on 16 Oct 2017, accepted on 28 Nov 2017 and first published on 28 Nov 2017


Article type: Communication
DOI: 10.1039/C7CC08004B
Citation: Chem. Commun., 2018, Advance Article
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    Rapid, enantioselective synthesis of the C1–C13 fragment of biselyngbyolide B

    R. G. Thorat and A. M. Harned, Chem. Commun., 2018, Advance Article , DOI: 10.1039/C7CC08004B

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