A copper-catalyzed cascade borylation/Petasis reaction for synthesis of regioselective 2 <i>H</i> -chromenes under catalytic amine conditions

We present a sustainable one-pot, copper-catalyzed synthesis of 2-phenyl-2 H -chromenes with excellent regioselectivity, requiring only a 0.5 mol% catalyst.

Authors

Yanqing Peng (ORCID: https://orcid.org/0000-0002-3811-7664)
Shuyan Wu (ORCID: https://orcid.org/0000-0001-9946-2720)
Gonghua Song (ORCID: https://orcid.org/0000-0002-4673-6561)
Jiayi Wang (ORCID: https://orcid.org/0000-0002-1313-138X)
Xiao-Ning Yang

Institutions

East China University of Science and Technology (CN)

Publication Details

Journal: Organic Chemistry Frontiers
Published: 2025-11-28
DOI: https://doi.org/10.1039/d5qo01398d
Primary Topic: Catalytic C–H Functionalization Methods
Type: article
Field-Weighted Citation Impact: 0.00

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article

A copper-catalyzed cascade borylation/Petasis reaction for synthesis of regioselective 2 H -chromenes under catalytic amine conditions

Yanqing Peng, Shuyan Wu, Gonghua Song, Jiayi Wang et al.

Nov 28, 2025

Organic Chemistry Frontiers

Catalytic C–H Functionalization Methods

article

A copper-catalyzed cascade borylation/Petasis reaction for synthesis of regioselective 2 H -chromenes under catalytic amine conditions

Yanqing Peng, Shuyan Wu, Gonghua Song, Jiayi Wang, Xiao-Ning Yang

November 28, 2025article en

Abstract

We present a sustainable one-pot, copper-catalyzed synthesis of 2-phenyl-2 H -chromenes with excellent regioselectivity, requiring only a 0.5 mol% catalyst.

Organic Chemistry FrontiersVol. 13(3)

East China University of Science and Technology (CN)

Openalex Percentile: Top 72%

Catalytic C–H Functionalization Methods

DOI Source OpenAlex

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