Issue 41, 2018

The synthesis of imidazo[1,5-a]quinolines via a decarboxylative cyclization under metal-free conditions

Abstract

An iodine-mediated decarboxylative cyclization was developed from α-amino acids and 2-methyl quinolines under metal-free conditions, affording a variety of imidazo[1,5-a]quinolines with moderate to good yields.

Graphical abstract: The synthesis of imidazo[1,5-a]quinolines via a decarboxylative cyclization under metal-free conditions

Supplementary files

Article information

Article type
Paper
Submitted
03 May 2018
Accepted
15 Jun 2018
First published
25 Jun 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 23058-23065

The synthesis of imidazo[1,5-a]quinolines via a decarboxylative cyclization under metal-free conditions

Z. Yan, C. Wan, Y. Yang, Z. Zha and Z. Wang, RSC Adv., 2018, 8, 23058 DOI: 10.1039/C8RA03786H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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