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Formal total synthesis of selaginpulvilin D

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Abstract

An efficient and mild synthetic strategy for the total synthesis of selaginpulvilin D has been reported. A highly chemoselective enyne–alkyne dehydro Diels–Alder reaction has been employed for the construction of the tricyclic fluorene framework present in the natural product selaginpulvilin D. An improved overall yield (10.5%) has been achieved for selaginpulvilin D, starting from commercially available m-anisaldehyde in 9 linear, operationally simple synthetic transformations.

Graphical abstract: Formal total synthesis of selaginpulvilin D

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Publication details

The article was received on 18 Apr 2017, accepted on 09 May 2017 and first published on 11 May 2017


Article type: Paper
DOI: 10.1039/C7OB00950J
Citation: Org. Biomol. Chem., 2017, Advance Article
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    Formal total synthesis of selaginpulvilin D

    B. S. Chinta and B. Baire, Org. Biomol. Chem., 2017, Advance Article , DOI: 10.1039/C7OB00950J

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