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Issue 8, 2012
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Enantioselective total synthesis of (+)-ibophyllidine via an asymmetric phosphine-catalyzed [3 + 2] annulation

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Abstract

In this study we performed the total synthesis of the terpene indole alkaloid (+)-ibophyllidine through a pathway involving asymmetric phosphine catalysis, with our novel L-4-hydroxyproline-derived chiral phosphine mediating the key [3 + 2] annulation. Hydrogenation of the [3 + 2] adduct allowed the rapid formation of the stereochemically dense pyrrolidine ring of (+)-ibophyllidine in excellent yield with exceptionally high levels of both diastereo- and enantioselectivity. We constructed the remainder of the pentacyclic skeleton through an intramolecular alkylation and an intramolecular aza-Morita–Baylis–Hillman reaction.

Graphical abstract: Enantioselective total synthesis of (+)-ibophyllidine via an asymmetric phosphine-catalyzed [3 + 2] annulation

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Publication details

The article was received on 18 Apr 2012, accepted on 19 May 2012 and first published on 23 May 2012


Article type: Edge Article
DOI: 10.1039/C2SC20468A
Citation: Chem. Sci., 2012,3, 2510-2514
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    Enantioselective total synthesis of (+)-ibophyllidine via an asymmetric phosphine-catalyzed [3 + 2] annulation

    I. P. Andrews and O. Kwon, Chem. Sci., 2012, 3, 2510
    DOI: 10.1039/C2SC20468A

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