CageCarbene‐Ir Complex Enables Selective Alkylation and Alkenylation of Benzyl Alcohols with Alkyl Sulfones

Comprehensive Summary A bis‐carbene iridium catalyst with a unique structure, featuring a straightforward synthetic route and low‐cost ligands was developed. This catalyst exhibits high catalytic activity in the Julia‐type olefination reactions between sulfone compounds and benzyl alcohol derivatives, with catalyst loading reduced to as low as 0.5 mol%. Furthermore, by adjusting the reaction conditions, the resultant olefinic products can be further reduced in a single step to afford the corresponding alkane compounds. This study also explores the reaction mechanism, proposing a plausible catalytic cycle based on a series of control experiments.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-10-18
DOI
https://doi.org/10.1002/cjoc.70297
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
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article

CageCarbene‐Ir Complex Enables Selective Alkylation and Alkenylation of Benzyl Alcohols with Alkyl Sulfones

Xuebing Leng, Lu Long, Yi‐Yan Yang, Weikang Jiang et al.
Chinese Journal of Chemistry
Asymmetric Hydrogenation and Catalysis
article

CageCarbene‐Ir Complex Enables Selective Alkylation and Alkenylation of Benzyl Alcohols with Alkyl Sulfones

Xuebing Leng, Lu Long, Yi‐Yan Yang, Weikang Jiang, Qilong Shen
article en

Abstract

Comprehensive Summary A bis‐carbene iridium catalyst with a unique structure, featuring a straightforward synthetic route and low‐cost ligands was developed. This catalyst exhibits high catalytic activity in the Julia‐type olefination reactions between sulfone compounds and benzyl alcohol derivatives, with catalyst loading reduced to as low as 0.5 mol%. Furthermore, by adjusting the reaction conditions, the resultant olefinic products can be further reduced in a single step to afford the corresponding alkane compounds. This study also explores the reaction mechanism, proposing a plausible catalytic cycle based on a series of control experiments.

Chinese Journal of ChemistryVol. 43(24)
New York University Shanghai (CN), Shanghai Advanced Research Institute (CN)
Openalex Percentile: Top 75%
Asymmetric Hydrogenation and Catalysis
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CageCarbene‐Ir Complex Enables Selective Alkylation and Alkenylation of Benzyl Alcohols with Alkyl Sulfones — Xuebing Leng, Lu Long, et al. · Chinese Journal of Chemistry (2025) | TGRS Research Map | TGRS