Nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles

A nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles has been established for the efficient synthesis of ( Z ) N -aryl β-enamino esters. 5-Alkoxy/phenoxy isoxazoles serve as reliable aminating reagents in this transformation through N–O bond cleavage. A wide range of N -aryl β...

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Veröffentlicht in:Organic Chemistry Frontiers 2024-09, Vol.11 (18), p.5138-5143
Hauptverfasser: Zhao, Yupeng, Wu, Changshu, Zhang, Jiaming, Gao, Yang, Yuan, Zhuoxuan, Li, Xianwei, Chen, Qian, Huo, Yanping
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Sprache:eng
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Zusammenfassung:A nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles has been established for the efficient synthesis of ( Z ) N -aryl β-enamino esters. 5-Alkoxy/phenoxy isoxazoles serve as reliable aminating reagents in this transformation through N–O bond cleavage. A wide range of N -aryl β-enamino esters (32 examples in up to 93% yields) with different functional groups were synthesized through this method under mild reaction conditions.
ISSN:2052-4129
2052-4110
2052-4129
2052-4110
DOI:10.1039/D4QO01050G