Photo-induced alkylation of benzil with trialkyltin chlorides

Abstract Despite its higher oxidation potential, Bu3SnCl has been found to be a more effective Bu-transferring reagent than Bu4Sn in the photo-induced reaction of benzil in benzene. The attractive interaction between Bu3SnCl and benzil, especially in benzene, is a presumable reason for its higher reactivity. In contrast, Bu2SnCl2 and BuSnCl3 are poorly reactive in such a photoreaction.

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Publication Details

Journal
Chemistry Letters
Published
2026-02-27
DOI
https://doi.org/10.1093/chemle/upag033
Primary Topic
Organometallic Compounds Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
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article

Photo-induced alkylation of benzil with trialkyltin chlorides

Yutaka Nishigaichi, S. IKEDA, Yoshiki Goto
Chemistry Letters
Organometallic Compounds Synthesis and Characterization
article

Photo-induced alkylation of benzil with trialkyltin chlorides

Yutaka Nishigaichi, S. IKEDA, Yoshiki Goto
article en

Abstract

Abstract Despite its higher oxidation potential, Bu3SnCl has been found to be a more effective Bu-transferring reagent than Bu4Sn in the photo-induced reaction of benzil in benzene. The attractive interaction between Bu3SnCl and benzil, especially in benzene, is a presumable reason for its higher reactivity. In contrast, Bu2SnCl2 and BuSnCl3 are poorly reactive in such a photoreaction.

Chemistry LettersVol. 55(3)
Shimane University (JP)
Openalex Percentile: Top 39%
Organometallic Compounds Synthesis and Characterization
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