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 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0035-1561614 |