Suzuki–Miyaura/Mizoroki–Heck coupling cascade to access 2,2′-bifunctionalized biaryls

Biaryl motifs are essential structural features in several drugs and functional molecules. Cyclic diaryliodonium has been scarcely explored as a bifunctional agent compared to ring opening and annulation reactions. Herein, a three-component cascade approach is developed to synthesize bifunctionalized biaryls employing cyclic diaryliodoniums as a biarylating agent. The mild conditions enabled a vast array of biarylated products in good yields in a single step. Furthermore, preliminary mechanistic details and photophysical properties have been investigated.

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Publication Details

Journal
Chemical Communications
Published
2024-12-23
DOI
https://doi.org/10.1039/d4cc05763e
Citations
3
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
0.75

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Suzuki–Miyaura/Mizoroki–Heck coupling cascade to access 2,2′-bifunctionalized biaryls

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3 citations
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article

Suzuki–Miyaura/Mizoroki–Heck coupling cascade to access 2,2′-bifunctionalized biaryls

Ruchir Kant, Naveen Kumar Maurya, Asit Kumar, Malleswara Rao Kuram, Ankita Sahu, Vishal Govind Rao, Ajeet Kumar Singh, Sanjeev K. Shukla
article en
3 citations

Abstract

Biaryl motifs are essential structural features in several drugs and functional molecules. Cyclic diaryliodonium has been scarcely explored as a bifunctional agent compared to ring opening and annulation reactions. Herein, a three-component cascade approach is developed to synthesize bifunctionalized biaryls employing cyclic diaryliodoniums as a biarylating agent. The mild conditions enabled a vast array of biarylated products in good yields in a single step. Furthermore, preliminary mechanistic details and photophysical properties have been investigated.

Chemical CommunicationsVol. 61(8)
Central Drug Research Institute (IN), Indian Institute of Technology Kanpur (IN), Academy of Scientific and Innovative Research (IN)
Science and Engineering Research Board
Openalex Percentile: Top 31%
Chemical synthesis and alkaloids
0.75
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