Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines

We report the synthesis of a series of alkylated indolizine derivatives from indolizine and <i>p</i>-QMs under ball-milling conditions. This method offers a controllable approach to synthesize mono- or di-alkenylated indolizines through modulation of substrate ratios, acid additives, and oxidant types. This procedure is solvent-free and operationally simple, and exhibits broad substrate tolerance, high conversion efficiency, and excellent scalability, making it both practical and versatile.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc05156h
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
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article

Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines

Yan‐Long Ma, Hua Cao, Yue Yu, Chunying Zhao et al.
Chemical Communications
Synthesis and Reactivity of Heterocycles
article

Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines

Yan‐Long Ma, Hua Cao, Yue Yu, Chunying Zhao, Ning Guan
article en

Abstract

We report the synthesis of a series of alkylated indolizine derivatives from indolizine and <i>p</i>-QMs under ball-milling conditions. This method offers a controllable approach to synthesize mono- or di-alkenylated indolizines through modulation of substrate ratios, acid additives, and oxidant types. This procedure is solvent-free and operationally simple, and exhibits broad substrate tolerance, high conversion efficiency, and excellent scalability, making it both practical and versatile.

Chemical CommunicationsVol. 61(86)
Guangdong Pharmaceutical University (CN)
Openalex Percentile: Top 79%
Synthesis and Reactivity of Heterocycles
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