Issue 53, 2017

Regioselective addition of C(sp3)–H bonds of alkyl pyridines to olefins catalysed by cationic zirconium complexes

Abstract

In situ generated cationic zirconium complexes stabilized by amine-bridged bis(phenolato) ligands have been developed to catalyse C(sp3)–H addition of alkyl pyridines to olefins, which are the first examples of group 4 metal based catalysts in this transformation. Ligand-controlled regioselectivity was observed, which was verified by DFT study.

Graphical abstract: Regioselective addition of C(sp3)–H bonds of alkyl pyridines to olefins catalysed by cationic zirconium complexes

Supplementary files

Article information

Article type
Communication
Submitted
01 شعبان 1438
Accepted
13 رمضان 1438
First published
13 رمضان 1438

Chem. Commun., 2017,53, 7401-7404

Regioselective addition of C(sp3)–H bonds of alkyl pyridines to olefins catalysed by cationic zirconium complexes

Q. Sun, P. Xie, D. Yuan, Y. Xia and Y. Yao, Chem. Commun., 2017, 53, 7401 DOI: 10.1039/C7CC03263C

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