Ruthenium‐catalyzed asymmetric ene‐yne metathesis

The first studies on [Ru]‐catalyzed Asymmetric Ring‐Closing Ene‐Yne Metathesis (ARCEYM) are disclosed in this communication. The desymmetrization of achiral ene‐diyne substrates afforded the corresponding exo cyclic compounds in good yields and enantioselectivities (up to 69 % ee). The methodology p...

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Veröffentlicht in:ChemCatChem 2024-04, Vol.16 (7), p.n/a
Hauptverfasser: Liu, Meng, Pearson‐Long, Morwenna S. M., Bertus, Philippe, Boeda, Fabien
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Sprache:eng
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Zusammenfassung:The first studies on [Ru]‐catalyzed Asymmetric Ring‐Closing Ene‐Yne Metathesis (ARCEYM) are disclosed in this communication. The desymmetrization of achiral ene‐diyne substrates afforded the corresponding exo cyclic compounds in good yields and enantioselectivities (up to 69 % ee). The methodology provided a straightforward access to functionalized scaffolds displaying alkyne and diene useful for further functionalization such as [4+2] cycloaddition reaction. The first studies on [Ru]‐catalyzed Asymmetric Ring‐Closing Ene‐Yne Metathesis (ARCEYM) are disclosed in this communication. The desymmetrization of achiral ene‐diyne substrates afforded the corresponding exo cyclic compounds in good yields and enantioselectivities (up to 69 % ee). The methodology provided a straightforward access to functionalized scaffolds displaying alkyne and diene useful for further functionalization such as [4+2] cycloaddition reaction.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.202301236