Rhodium-catalyzed cycloaddition of bicyclo[1.1.0]butanes with <i>N</i> , <i>N</i> ′-cyclic azomethine imines: <i>en route</i> to fused diaza-3D scaffolds

The construction of aza-3D frameworks has emerged as a pivotal strategy in drug discovery, owing to their ability to mimic heteroarene bioisosteres.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo01147g
Citations
1
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.94
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article

Rhodium-catalyzed cycloaddition of bicyclo[1.1.0]butanes with N , N ′-cyclic azomethine imines: en route to fused diaza-3D scaffolds

Kun Yin, Yuting Shen, Qiang Qin, Jian Li et al.
1 citations
Organic Chemistry Frontiers
Cyclopropane Reaction Mechanisms
0.94
article

Rhodium-catalyzed cycloaddition of bicyclo[1.1.0]butanes with N , N ′-cyclic azomethine imines: en route to fused diaza-3D scaffolds

Kun Yin, Yuting Shen, Qiang Qin, Jian Li, Jin Li, Zixi Wang, Xinyao Li, Zijun Zhou, Tianlei Du
article en
1 citations

Abstract

The construction of aza-3D frameworks has emerged as a pivotal strategy in drug discovery, owing to their ability to mimic heteroarene bioisosteres.

Organic Chemistry FrontiersVol. 12(24)
Shanghai University (CN), Fuyang Normal University (CN)
Openalex Percentile: Top 22%
Cyclopropane Reaction Mechanisms
0.94
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