Advances and Setbacks in the Total Synthesis of the Fungal Metabolite Curvicollide C: Synthesis and Elaboration of Non-Aldol Stereotriads from Gosteli-Type Allyl Vinyl Ethers

Abstract Advances and setbacks are reported in regard to the asymmetric total synthesis of the fungal metabolite curvicollide C relying on a synthetic strategy that exploits non-aldol stereotriads as chiral building blocks. A catalytic asymmetric Gosteli–Claisen rearrangement, a two-step aldehyde-to...

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Veröffentlicht in:Synthesis (Stuttgart) 2016-08, Vol.48 (15), p.2466-2482
Hauptverfasser: Körner, Marleen, Hiersemann, Martin
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract Advances and setbacks are reported in regard to the asymmetric total synthesis of the fungal metabolite curvicollide C relying on a synthetic strategy that exploits non-aldol stereotriads as chiral building blocks. A catalytic asymmetric Gosteli–Claisen rearrangement, a two-step aldehyde-to-alkyne-homologation, and a Julia–Kocienski olefination served as key C/C-connecting transformations.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0035-1561614