Issue 6, 2018

ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols

Abstract

Various Ru(II) complexes bearing functionalized 2,2′-bipyridine ligands were synthesized and fully characterized. Among them, a new N6,N6′-dimethyl-2,2′-bipyridine-6,6′-diamine ligand was found to be the most electron-rich ligand as its corresponding Ru(II) complex (1a) displayed the lowest νco value and the highest efficiency in the β-alkylation of secondary alcohols with primary alcohols (TON = 98 860). Complex 1a also exhibited a greater reactivity in the monoalkylation of acetonitrile, α-alkylation as well as α-methylation of arylacetonitriles. Compared to the other reported systems, in α-methylation of nitriles complex 1a presented superior catalytic activity. The potential of complex 1a was extended further in N-methylation of amines using methanol as a green methylating agent.

Graphical abstract: ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols

Supplementary files

Article information

Article type
Research Article
Submitted
28 নভে. 2017
Accepted
03 জানু. 2018
First published
03 জানু. 2018

Org. Chem. Front., 2018,5, 1008-1018

ortho-Amino group functionalized 2,2′-bipyridine based Ru(II) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols

B. C. Roy, S. Debnath, K. Chakrabarti, B. Paul, M. Maji and S. Kundu, Org. Chem. Front., 2018, 5, 1008 DOI: 10.1039/C7QO01061C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements