Regiocontrollable B(2/3)–H Alkenylation of nido-Carboranes

Anionic nido-carboranes, as open-cage analogues of closo-carboranes with strong hydrophilicity and higher potential in the development of biomedicines, have been notably more challenging because of their strong interaction with transition metals. While the exo-cage B–H activation reactions of nido-c...

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Veröffentlicht in:Organic letters 2024-09, Vol.26 (38), p.8134-8138
Hauptverfasser: Li, Ping, Yang, Jiayi, Zeng, Jiayi, Miao, Shuqing, Fang, Ran, Lu, Jian, Lu, Ju-You
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Sprache:eng
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