Issue 8, 2017

A direct metal-free C2–H functionalization of quinoline N-oxides: a highly selective amination and alkylation strategy towards 2-substituted quinolines

Abstract

An efficient one-pot methodology for C2-selective amination and alkylation of quinoline N-oxides towards 2-substituted quinolines was developed, via the reaction of various quinoline N-oxides with ammonia, a large variety of primary and secondary amines, as well as active methylene compounds in the presence of diethyl H-phosphonate and K2CO3 under metal free conditions at room temperature.

Graphical abstract: A direct metal-free C2–H functionalization of quinoline N-oxides: a highly selective amination and alkylation strategy towards 2-substituted quinolines

Supplementary files

Article information

Article type
Research Article
Submitted
21 Apr 2017
Accepted
10 May 2017
First published
11 May 2017

Org. Chem. Front., 2017,4, 1595-1600

A direct metal-free C2–H functionalization of quinoline N-oxides: a highly selective amination and alkylation strategy towards 2-substituted quinolines

W. Bi, K. Sun, C. Qu, X. Chen, L. Qu, S. Zhu, X. Li, H. Wu, L. Duan and Y. Zhao, Org. Chem. Front., 2017, 4, 1595 DOI: 10.1039/C7QO00311K

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