Rh-catalyzed [3 + 2] cyclization of (hetero)cyclic 1,3-dicarbonyls with 2-aminoarylboronic esters to access carbazolones

The first Suzuki-type [3 + 2] cyclization of cyclic 1,3-dicarbonyls with 2-aminoarylboronic esters has been developed. With eco-friendly EtOH/H 2 O as solvent, a series of structurally and electronically diverse carbazolones can be readily obtained.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo01079a
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Rh-catalyzed [3 + 2] cyclization of (hetero)cyclic 1,3-dicarbonyls with 2-aminoarylboronic esters to access carbazolones

Zhonghua Gu, Feng Qiu, Hui Xiong, Bei Wan et al.
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
article

Rh-catalyzed [3 + 2] cyclization of (hetero)cyclic 1,3-dicarbonyls with 2-aminoarylboronic esters to access carbazolones

Zhonghua Gu, Feng Qiu, Hui Xiong, Bei Wan, Shaoyu Mai, Yi Deng, Ce Liu, Qingfeng Du
article en

Abstract

The first Suzuki-type [3 + 2] cyclization of cyclic 1,3-dicarbonyls with 2-aminoarylboronic esters has been developed. With eco-friendly EtOH/H 2 O as solvent, a series of structurally and electronically diverse carbazolones can be readily obtained.

Organic Chemistry FrontiersVol. 12(24)
Guangzhou University of Chinese Medicine (CN), Third Affiliated Hospital of Southern Medical University (CN), TCM-Intigrated Cancer Center of Southern Medical University (CN), Southern Medical University (CN)
Openalex Percentile: Top 80%
Catalytic C–H Functionalization Methods
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