Base-Mediated Substrate-Dependent [2 + 3] and [3 + 3] Annulation of Bisnucleophiles: Enabling the Modular Synthesis of Functionalized Spirocyclopentane Oxindoles and Tetrahydro-α-carbolines

Herein, we represented two facile and efficient approaches for the synthesis of functionalized spirocyclopentane oxindoles and tetrahydro-α-carbolines from different bisnucleophiles with 3-iodo-2-iodomethyl-1-propene via [2 + 3] and [3 + 3] annulation. These methods exhibit good functional group tolerances, simple conditions, easily available start materials, and moderate to good yields.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-07-16
DOI
https://doi.org/10.1021/acs.joc.5c00899
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
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article

Base-Mediated Substrate-Dependent [2 + 3] and [3 + 3] Annulation of Bisnucleophiles: Enabling the Modular Synthesis of Functionalized Spirocyclopentane Oxindoles and Tetrahydro-α-carbolines

Jiaxu Feng, XiangDi Wang, Lulu Xu, Yingying Wu
1 links
The Journal of Organic Chemistry
Asymmetric Synthesis and Catalysis
article

Base-Mediated Substrate-Dependent [2 + 3] and [3 + 3] Annulation of Bisnucleophiles: Enabling the Modular Synthesis of Functionalized Spirocyclopentane Oxindoles and Tetrahydro-α-carbolines

Jiaxu Feng, XiangDi Wang, Lulu Xu, Yingying Wu
article en

Abstract

Herein, we represented two facile and efficient approaches for the synthesis of functionalized spirocyclopentane oxindoles and tetrahydro-α-carbolines from different bisnucleophiles with 3-iodo-2-iodomethyl-1-propene via [2 + 3] and [3 + 3] annulation. These methods exhibit good functional group tolerances, simple conditions, easily available start materials, and moderate to good yields.

The Journal of Organic ChemistryVol. 90(29)
Tianjin University of Science and Technology (CN), College of Medical Sciences (NP), Biobase (Germany) (DE)
Openalex Percentile: Top 87%
Asymmetric Synthesis and Catalysis
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