Alkoxide Base-Mediated Methyl Boration of Aryl Alkenes and Arylidenecyclopropanes

Abstract A transition-metal-free methyl boration of aryl alkenes with B2pin2 and methyl iodide has been achieved using the alkoxide base tBuOK as the sole mediator. In contrast, previous alkene methyl borations employ transition-metal catalysts. Apart from styrenes, arylidenecyclopropanes have also been found to undergo efficient transformations with the retention of the cyclopropyl rings for the synthesis of tertiary boronates. Mechanistic investigations revealed the involvement of an anionic intermediate in the reaction process.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-09-11
DOI
https://doi.org/10.1021/acs.joc.6c00602
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Alkoxide Base-Mediated Methyl Boration of Aryl Alkenes and Arylidenecyclopropanes

Lipeng Wu, Ximei Tian
The Journal of Organic Chemistry
Organoboron and organosilicon chemistry
article

Alkoxide Base-Mediated Methyl Boration of Aryl Alkenes and Arylidenecyclopropanes

Lipeng Wu, Ximei Tian
article en

Abstract

Abstract A transition-metal-free methyl boration of aryl alkenes with B2pin2 and methyl iodide has been achieved using the alkoxide base tBuOK as the sole mediator. In contrast, previous alkene methyl borations employ transition-metal catalysts. Apart from styrenes, arylidenecyclopropanes have also been found to undergo efficient transformations with the retention of the cyclopropyl rings for the synthesis of tertiary boronates. Mechanistic investigations revealed the involvement of an anionic intermediate in the reaction process.

The Journal of Organic Chemistry
Tianjin University (CN), Lanzhou Institute of Chemical Physics (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 20%
Organoboron and organosilicon chemistry
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