Nickel(II)-Catalyzed Borylation of Alkenyl Methyl Ethers via C–O Bond Cleavage

A new protocol has been developed for the borylation of conjugated alkenyl methyl ethers using B2Pin2 via C–O bond cleavage catalyzed by Ni­(II). In this cross-coupling reaction, both E/Z isomers of alkenyl ethers are converted into (E)-alkenyl boronic esters with good reactivity. This transformatio...

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Veröffentlicht in:Organic letters 2020-08, Vol.22 (16), p.6424-6428
Hauptverfasser: Qiu, Xiaodong, Li, Yangyang, Zhou, Li, Chen, Peishan, Li, Fan, Zhang, Yanan, Ling, Yong
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Sprache:eng
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Zusammenfassung:A new protocol has been developed for the borylation of conjugated alkenyl methyl ethers using B2Pin2 via C–O bond cleavage catalyzed by Ni­(II). In this cross-coupling reaction, both E/Z isomers of alkenyl ethers are converted into (E)-alkenyl boronic esters with good reactivity. This transformation exhibits high chemoselectivity in the presence of competitive C–O bonds such as aryl ether, ester, amide, and thioether groups, thus providing a new method for the construction of various alkenyl boronates.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.0c02236