Rh(III)-Catalyzed Regioselective B(4)–H Alkylation of <i>o</i> -Carboranes with Alkenes

Herein, we describe a versatile Rh(III)-catalyzed platform for the exclusive B(4)-H alkylation of <i>o</i>-carborane, needing only one equivalent of alkenes (40 examples, up to 90% yield). Notably, this approach deviates significantly from established pathways that typically yield alkenylated products in carborane-alkene reactions. Mechanistic analysis indicates that monoalkylation selectivity is kinetically regulated by the post-coordination of the monoalkylated product to Rh(III).

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Publication Details

Journal
Organic Letters
Published
2025-10-23
DOI
https://doi.org/10.1021/acs.orglett.5c03574
Citations
1
Primary Topic
Boron Compounds in Chemistry
Type
article
Field-Weighted Citation Impact
1.36
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Rh(III)-Catalyzed Regioselective B(4)–H Alkylation of o -Carboranes with Alkenes

Hou‐Ji Cao, Hong Yan, Qianyi Zhao, Meijiu Liu et al.
1 citations
Organic Letters
Boron Compounds in Chemistry
1.36
article

Rh(III)-Catalyzed Regioselective B(4)–H Alkylation of o -Carboranes with Alkenes

Hou‐Ji Cao, Hong Yan, Qianyi Zhao, Meijiu Liu, Jiaxin Li, Jia-Hui Yan, Ju Zhang, Mingwei Zhao, R. Ma
article en
1 citations

Abstract

Herein, we describe a versatile Rh(III)-catalyzed platform for the exclusive B(4)-H alkylation of <i>o</i>-carborane, needing only one equivalent of alkenes (40 examples, up to 90% yield). Notably, this approach deviates significantly from established pathways that typically yield alkenylated products in carborane-alkene reactions. Mechanistic analysis indicates that monoalkylation selectivity is kinetically regulated by the post-coordination of the monoalkylated product to Rh(III).

Organic LettersVol. 27(44)
Henan Normal University (CN), Nanjing University (CN)
Openalex Percentile: Top 15%
Boron Compounds in Chemistry
1.36
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Rh(III)-Catalyzed Regioselective B(4)–H Alkylation of <i>o</i> -Carboranes with Alkenes — Hou‐Ji Cao, Hong Yan, et al. · Organic Letters (2025) | TGRS Research Map | TGRS