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Transition-metal-catalyzed aminometalation of -alkynylanilines is a promising pathway for the synthesis of C3-functionalized indoles. Herein, we describe the Cu(II)-catalyzed site-selective C3-heteroarylation of indoles from -alkynylanilines and quinoline -oxides. A plausible reaction mechanism involving the aminocupration of -alkynylanilines followed by the nucleophilic addition of Cu(II)-indolyl complexes to quinoline -oxides was proposed. Post-transformations of the generated C3-heteroarylated indoles demonstrated the broad applicability of the developed method.
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http://dx.doi.org/10.1021/acs.joc.5c00007 | DOI Listing |
J Org Chem
March 2025
School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Transition-metal-catalyzed aminometalation of -alkynylanilines is a promising pathway for the synthesis of C3-functionalized indoles. Herein, we describe the Cu(II)-catalyzed site-selective C3-heteroarylation of indoles from -alkynylanilines and quinoline -oxides. A plausible reaction mechanism involving the aminocupration of -alkynylanilines followed by the nucleophilic addition of Cu(II)-indolyl complexes to quinoline -oxides was proposed.
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