tert-Butyl peroxybenzoate (TBPB)-mediated 2-isocyanobiaryl insertion with 1,4-dioxane: efficient synthesis of 6-alkyl phenanthridines via C(sp3)-H/C(sp2)-H bond functionalization.

Chem Commun (Camb)

Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.

Published: June 2014

An efficient method for the construction of 6-alkyl phenanthridines by tert-butyl peroxybenzoate (TBPB)-mediated 2-isocyanobiaryl insertion with 1,4-dioxane was established. Two new C-C bonds were formed in this reaction via a sequential C(sp(3))-H/C(sp(2))-H bond functionalization under metal-free conditions.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c4cc00743cDOI Listing

Publication Analysis

Top Keywords

tert-butyl peroxybenzoate
8
peroxybenzoate tbpb-mediated
8
tbpb-mediated 2-isocyanobiaryl
8
2-isocyanobiaryl insertion
8
insertion 14-dioxane
8
6-alkyl phenanthridines
8
csp3-h/csp2-h bond
8
bond functionalization
8
14-dioxane efficient
4
efficient synthesis
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!