Issue 21, 2024

Cu2O-catalyzed cascade phosphinylation/cyclization of 2′-aminochalcones for the synthesis of hemi-indigo derivatives

Abstract

A Cu2O-catalyzed cascade phosphinylation/cyclization reaction of 2′-aminochalcones and diphenylphosphine oxides to produce hemi-indigo derivatives has been developed. This strategy facilitates the sequential formation of a C–P bonds and a C–N bond in a single reaction step. Notably, the approach features one-pot operation, an earth-abundant copper catalyst, readily available starting materials, a broad substrate scope and high compatibility with functional groups, providing 33 compounds in acceptable yields.

Graphical abstract: Cu2O-catalyzed cascade phosphinylation/cyclization of 2′-aminochalcones for the synthesis of hemi-indigo derivatives

Supplementary files

Article information

Article type
Communication
Submitted
11 Apr 2024
Accepted
02 May 2024
First published
08 May 2024

Org. Biomol. Chem., 2024,22, 4249-4253

Cu2O-catalyzed cascade phosphinylation/cyclization of 2′-aminochalcones for the synthesis of hemi-indigo derivatives

X. Liu, L. Hao, Y. Wang, X. Yu, Z. Yang, Y. Liu and Y. Ji, Org. Biomol. Chem., 2024, 22, 4249 DOI: 10.1039/D4OB00594E

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