Copper(I)-Catalyzed Stereoselective Synthesis of 4-(Aminomethylene)-1,4-dihydroisoquinolin-3-ones from 4-Diazo-1,4-dihydroisoquinolin-3-ones and Thioamides

)-configuration. The versatility and selectivity of this protocol highlight its potential utility in organic synthesis.

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Publication Details

Journal
ACS Omega
Published
2026-04-15
DOI
https://doi.org/10.1021/acsomega.6c01111
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Copper(I)-Catalyzed Stereoselective Synthesis of 4-(Aminomethylene)-1,4-dihydroisoquinolin-3-ones from 4-Diazo-1,4-dihydroisoquinolin-3-ones and Thioamides

Xin Hong, YanGuang Wang, Ping Lü, Jiale Fan et al.
ACS Omega
Catalytic C–H Functionalization Methods
article

Copper(I)-Catalyzed Stereoselective Synthesis of 4-(Aminomethylene)-1,4-dihydroisoquinolin-3-ones from 4-Diazo-1,4-dihydroisoquinolin-3-ones and Thioamides

Xin Hong, YanGuang Wang, Ping Lü, Jiale Fan, Yingxiao Wang, Tian-Yi Chen
article en

Abstract

)-configuration. The versatility and selectivity of this protocol highlight its potential utility in organic synthesis.

ACS OmegaVol. 11(16)
Zhejiang University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 29%
Catalytic C–H Functionalization Methods
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