Enantioselective BIMP-catalysed [2,3]-Wittig Rearrangements of Oxindole-Derived Allylic and Propargylic Ethers

The organocatalytic enantioselective [2,3]-Wittig rearrangement of a range of oxindole-derived allylic and propargylic ethers using bifunctional iminophosphorane (BIMP) organosuperbase catalysts has been investigated, generating 3-hydroxyoxindole derivatives in high stereoselectivity (>35...

Publication Details

Journal: Organic Chemistry Frontiers
Published: 2026-01-01
DOI: https://doi.org/10.1039/d6qo00342g
Primary Topic: Asymmetric Synthesis and Catalysis
Type: article
Field-Weighted Citation Impact: 0.00

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article

Enantioselective BIMP-catalysed [2,3]-Wittig Rearrangements of Oxindole-Derived Allylic and Propargylic Ethers

Jan 1, 2026

Organic Chemistry Frontiers

Asymmetric Synthesis and Catalysis

article

Enantioselective BIMP-catalysed [2,3]-Wittig Rearrangements of Oxindole-Derived Allylic and Propargylic Ethers

January 1, 2026article en

Abstract

Organic Chemistry Frontiers

Openalex Percentile: Top 10%

Asymmetric Synthesis and Catalysis

DOI Open Access PDF OpenAlex

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Enantioselective BIMP-catalysed [2,3]-Wittig Rearrangements of Oxindole-Derived Allylic and Propargylic Ethers · Organic Chemistry Frontiers (2026) | TGRS Research Map | TGRS