Transition-metal-free direct alkylation of aryl tetrazoles via intermolecular oxidative C-N formation.

J Org Chem

School of Petrochemical Engineering and Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, Changzhou University, Changzhou, 213164, P. R. China.

Published: December 2014

A transition-metal-free synthetic approach for constructing alkylated aryl tetrazoles has been developed using n-Bu4NI as the catalyst and t-BuOOH as the oxidant. It involves the direct C-N bond formation through sp(3) C-H activation. A wide range of benzylic C-H substrates (or alkyl ethers) and aryl tetrazoles undergo this reaction smoothly to deliver the corresponding products in good yields.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jo502283hDOI Listing

Publication Analysis

Top Keywords

aryl tetrazoles
12
transition-metal-free direct
4
direct alkylation
4
alkylation aryl
4
tetrazoles intermolecular
4
intermolecular oxidative
4
oxidative c-n
4
c-n formation
4
formation transition-metal-free
4
transition-metal-free synthetic
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!