Fickle Reactivity of Allenes in Transition‐Metal‐Catalyzed C−H Functionalizations
Transition‐metal‐catalyzed C−H functionalizations with allenes lead to unique selectivity challenges due to the presence of two adjacent carbon–carbon double bonds, which enables a series of atom‐ and step‐economical alkenylation, allenylation, allylation, dienylation, and annulation reactions of di...
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Veröffentlicht in: | Asian journal of organic chemistry 2018-07, Vol.7 (7), p.1151-1163 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Transition‐metal‐catalyzed C−H functionalizations with allenes lead to unique selectivity challenges due to the presence of two adjacent carbon–carbon double bonds, which enables a series of atom‐ and step‐economical alkenylation, allenylation, allylation, dienylation, and annulation reactions of different substrates. This Focus Review highlights the recent remarkable advancements made in transition‐metal‐catalyzed C−H functionalization with allenes.
The magic of allenes: This Focus Review highlights the variable reactivity of allenes for alkenylation, allenylation, allylation and annulation reactions by transition‐metal‐catalyzed C−H activation. |
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ISSN: | 2193-5807 2193-5815 |
DOI: | 10.1002/ajoc.201800133 |