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Total Synthesis of Selaginpulvilins A and C

Abstract

An efficient formal total synthesis of selaginpulvilin family of natural products selaginpulvilin A and C has been successfully achieved. The tetradehydro Diels-Alder (TDDA) reaction between an enyne and alkyne has been utilized for the creation of necessary fluorene skeleton. Attempts for the conversion of selaginpulvilin A to selaginpulvilin B, F and H were unsuccessful.

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Publication details

The article was received on 24 Oct 2017, accepted on 01 Dec 2017 and first published on 01 Dec 2017


Article type: Paper
DOI: 10.1039/C7OB02609A
Citation: Org. Biomol. Chem., 2017, Accepted Manuscript
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    Total Synthesis of Selaginpulvilins A and C

    B. Baire and B. S. Chinta, Org. Biomol. Chem., 2017, Accepted Manuscript , DOI: 10.1039/C7OB02609A

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