Palladium-catalyzed diastereoselective cross-coupling of two aryl halides via C-H activation: synthesis of chiral eight-membered nitrogen heterocycles

A method for the synthesis of enantiopure eight-membered nitrogen heterocycles has been developed through diastereoselective cross-coupling of 2-iodobiphenyls with 2-bromobenzylamines. The products represent a novel type of chiral scaffold, which feature easy modification and high configurative stab...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2021-03, Vol.57 (23), p.2939-2942
Hauptverfasser: Cheng, Cang, Zuo, Xiang, Tu, Dongdong, Wan, Bin, Zhang, Yanghui
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Sprache:eng
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Zusammenfassung:A method for the synthesis of enantiopure eight-membered nitrogen heterocycles has been developed through diastereoselective cross-coupling of 2-iodobiphenyls with 2-bromobenzylamines. The products represent a novel type of chiral scaffold, which feature easy modification and high configurative stability and have the potential to be applied in asymmetric synthesis. Palladacycles that were formed via the C-H activation of 2-iodobiphenyls should act as the intermediates. The reaction provides a new strategy for the synthesis of medium-sized ring compounds.
ISSN:1359-7345
1364-548X
DOI:10.1039/d1cc00398d