Gold-catalyzed regioselective remote B(9)-H activation of o-carboranes with silylenynones: access to B(9)-α-furylsilyl-o-carboranes

The gold-catalyzed regioselective remote B(9)-H functionalization of o-carboranes through regioselective insertion of α-furyl silyl gold carbenes generated from silylenynones into the B(9)-H bond of o-carboranes offers facile and atom-economical access to various B(9)-α-furylsilyl-o-carboranes in mo...

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Auteurs principaux: Hao, Yue (Auteur) , Zheng, Huiyuan (Auteur) , Hang, Chengrui (Auteur) , Zhi, Ling (Auteur) , Hashmi, A. Stephen K. (Auteur) , Wang, Guanghui (Auteur) , Zhao, Ximei (Auteur)
Format: Article (Journal)
Langue:anglais
Publié: 10 April 2026
In: Organic letters
Year: 2026, Volume: 28, Numéro: 14, Pages: 4384-4389
ISSN:1523-7052
DOI:10.1021/acs.orglett.6c00507
Accès en ligne:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.orglett.6c00507
Verlag, lizenzpflichtig, Volltext: https://pubs.acs.org/doi/10.1021/acs.orglett.6c00507?src=getftr&utm_source=clarivate&getft_integrator=clarivate
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Notes sur l'auteur:Yue Hao, Huiyuan Zheng, Chengrui Hang, Ling Zhi, A. Stephen K. Hashmi, Guanghui Wang, Ximei Zhao
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Résumé:The gold-catalyzed regioselective remote B(9)-H functionalization of o-carboranes through regioselective insertion of α-furyl silyl gold carbenes generated from silylenynones into the B(9)-H bond of o-carboranes offers facile and atom-economical access to various B(9)-α-furylsilyl-o-carboranes in moderate to good yields (up to 88%) with excellent regioselectivities. This method can also be expanded to the selective B-H functionalization of m-carboranes. The synthetic potential of this methodology is exemplified by gram-scale experiments and synthetic transformations of the products.
Description:Online verfügbar: 27. März 2026
Gesehen am 02.06.2026
Description matérielle:Online Resource
ISSN:1523-7052
DOI:10.1021/acs.orglett.6c00507