RhIII–Catalyzed Direct Heteroarylation of Unactivated C(sp3)–H with N-Heteroaryl Boronates
Rong Chi,
Guang-Yu Xu,
Zhen-Ang Liu
et al.
Abstract:Disclosed herein is a rhodium(III)-catalyzed direct heteroarylation reaction between unactivated aliphatic C(sp 3 )−H bonds in 2-alkylpyridines and heteroaryl organoboron reagents. This catalytic protocol is compatible with various heterocyclic boronates containing ortho-and meta-pyridine, pyrazoles, furan, and quinoline with strong coordination capability. The achievement of this methodology provides an efficient route to build new C(sp 3 )−heteroaryl bonds.
The direct activation of inert saturated C-H bonds for selective functionalization has long been a significant challenge in organic synthesis. The past few decades have witnessed the emergence of visible-light...
The direct activation of inert saturated C-H bonds for selective functionalization has long been a significant challenge in organic synthesis. The past few decades have witnessed the emergence of visible-light...
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