Photoinduced Pd-Catalyzed Selective 1,4-Dicarbofunctionalization of 1,3-Butadiene with Alkyl or Aryl Bromides and Oxindoles

Abstract The dicarbofunctionalization of 1,3-butadiene provides rapid access to complex allyl compounds in organic synthesis. Here we report a photoinduced palladium-catalyzed three-component coupling that enables selective 1,4-dicarbofunctionalization of 1,3-butadiene with alkyl or aryl bromides and oxindole nucleophiles. This transformation utilizes photoexcited Pd(0) species to activate both substrate classes via single-electron transfer, accommodating radicals of distinctly different electronic nature—nucleophilic alkyl radicals and electrophilic aryl radicals—through tailored reaction conditions. Under mild conditions, the protocol delivers 80 oxindole derivatives in good yields (up to 93%) and regioselectivities (up to >20:1 r.r.), providing efficient access to bioactive oxindole scaffolds.

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Publication Details

Journal
Synthesis
Published
2025-10-17
DOI
https://doi.org/10.1055/a-2700-2940
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Photoinduced Pd-Catalyzed Selective 1,4-Dicarbofunctionalization of 1,3-Butadiene with Alkyl or Aryl Bromides and Oxindoles

Xiao‐Yun Ruan, Mostafa Sayed, Liu‐Zhu Gong, Zhi-Yong Han et al.
Synthesis
Catalytic C–H Functionalization Methods
article

Photoinduced Pd-Catalyzed Selective 1,4-Dicarbofunctionalization of 1,3-Butadiene with Alkyl or Aryl Bromides and Oxindoles

Xiao‐Yun Ruan, Mostafa Sayed, Liu‐Zhu Gong, Zhi-Yong Han, Dan-Xing Wu
article en

Abstract

Abstract The dicarbofunctionalization of 1,3-butadiene provides rapid access to complex allyl compounds in organic synthesis. Here we report a photoinduced palladium-catalyzed three-component coupling that enables selective 1,4-dicarbofunctionalization of 1,3-butadiene with alkyl or aryl bromides and oxindole nucleophiles. This transformation utilizes photoexcited Pd(0) species to activate both substrate classes via single-electron transfer, accommodating radicals of distinctly different electronic nature—nucleophilic alkyl radicals and electrophilic aryl radicals—through tailored reaction conditions. Under mild conditions, the protocol delivers 80 oxindole derivatives in good yields (up to 93%) and regioselectivities (up to >20:1 r.r.), providing efficient access to bioactive oxindole scaffolds.

SynthesisVol. 57(23)
South Valley University (EG), Hefei National Center for Physical Sciences at Nanoscale (CN), New Valley University
Openalex Percentile: Top 77%
Catalytic C–H Functionalization Methods
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