Issue 16, 2019

Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides

Abstract

Two new types of silver-catalyzed nitration–annulations of 2-alkynylanilines with tert-butyl nitrite (TBN) were reported, leading to the selective formation of a variety of nitrated indoles and indazole-2-oxides by changing the N-protection of 2-alkynylanilines. Ag-Catalyzed nitration–annulation of N-sulfonyl 2-alkynylanilines without C4 substituents afforded 5-nitroindoles under neutral-redox conditions, whereas the presence of C5 substituents gave 7-nitroindoles through silver catalysis. N-Methyl 2-alkynylanilines underwent a completely different process to furnish aroyl indazole-2-oxides.

Graphical abstract: Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides

Supplementary files

Article information

Article type
Research Article
Submitted
03 Jun 2019
Accepted
06 Jul 2019
First published
08 Jul 2019

Org. Chem. Front., 2019,6, 2968-2973

Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides

T. Zhang, R. Wang, P. Cai, W. Hao, S. Tu and B. Jiang, Org. Chem. Front., 2019, 6, 2968 DOI: 10.1039/C9QO00715F

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