Issue 12, 2002

Solid supported fluoronitroaryl triazenes as immobilized and convertible Sanger reagents – synthesis and SNAr reactions towards a novel preparation of 1-alkyl-5-nitro-1H-benzotriazoles

Abstract

Synthesis of novel fluoronitroaryl triazenes in liquid phase and on solid support have been described; mild displacement of the fluoride ion with various nucleophiles provides access to substituted arenes which in turn can be cleaved to provide a unique access to 1-alkyl-5-nitro-1H-benzotriazole.

Graphical abstract: Solid supported fluoronitroaryl triazenes as immobilized and convertible Sanger reagents – synthesis and SNAr reactions towards a novel preparation of 1-alkyl-5-nitro-1H-benzotriazoles

Supplementary files

Article information

Article type
Communication
Submitted
11 Feb 2002
Accepted
25 Mar 2002
First published
17 May 2002

Chem. Commun., 2002, 1296-1297

Solid supported fluoronitroaryl triazenes as immobilized and convertible Sanger reagents – synthesis and SNAr reactions towards a novel preparation of 1-alkyl-5-nitro-1H-benzotriazoles

M. E. P. Lormann, C. H. Walker, M. Es-Sayed and S. Bräse, Chem. Commun., 2002, 1296 DOI: 10.1039/B201489K

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