Cobalt-Mediated Reactions of Oxazoles and Thiazoles with Alkynes
Abstract An experimental foray into the potential of oxazoles and thiazoles to enter into CpCo-mediated [2+2+2] cycloadditions is described. α,ω-Diynes failed to engage the heterocycles productively, as illustrated by the behavior of the unique cobaltacyclopentadiene(oxazole) complex 10 , the isolat...
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Veröffentlicht in: | Synthesis (Stuttgart) 2015-11, Vol.47 (21), p.3412-3422 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
An experimental foray into the potential of oxazoles and thiazoles to enter into CpCo-mediated [2+2+2] cycloadditions is described. α,ω-Diynes failed to engage the heterocycles productively, as illustrated by the behavior of the unique cobaltacyclopentadiene(oxazole) complex
10
, the isolation and X-ray structural determination of which is recorded. Alkyne-tethered systems gave moderate yields to products resulting from [2+2+2] cycloaddition and C–H activation. The azaenol ether bridge in the cycloaddition products appears sensitive to oxidation, elimination, and rearrangement, depending on the system and reaction conditions. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0034-1378820 |