Issue 46, 2016

Bifunctional Ru(ii) complex catalysed carbon–carbon bond formation: an eco-friendly hydrogen borrowing strategy

Abstract

The atom economical borrowing hydrogen methodology enables the use of alcohols as alkylating agents for selective C–C bond formation. A bifunctional 2-(2-pyridyl-2-ol)-1,10-phenanthroline (phenpy-OH) based Ru(II) complex (2) was found to be a highly efficient catalyst for the one-pot β-alkylation of secondary alcohols with primary alcohols and double alkylation of cyclopentanol with different primary alcohols. Exploiting the metal–ligand cooperativity in complex 2, several aromatic, aliphatic and heteroatom substituted alcohols were selectively cross-coupled in high yields using significantly low catalyst loading (0.1 mol%). An outer-sphere mechanism is proposed for this system as exogenous PPh3 has no significant effect on the rate of the reaction. Notably, this is a rare one-pot strategy for β-alkylation of secondary alcohols using a bifunctional Ru(II)-complex. Moreover, this atom-economical methodology displayed the highest cumulative turn over frequency (TOF) among all the reported transition metal complexes in cross coupling of alcohols.

Graphical abstract: Bifunctional Ru(ii) complex catalysed carbon–carbon bond formation: an eco-friendly hydrogen borrowing strategy

Supplementary files

Article information

Article type
Paper
Submitted
12 ذو الحجة 1437
Accepted
29 محرم 1438
First published
01 صفر 1438

Org. Biomol. Chem., 2016,14, 10988-10997

Bifunctional Ru(II) complex catalysed carbon–carbon bond formation: an eco-friendly hydrogen borrowing strategy

K. Chakrabarti, B. Paul, M. Maji, B. C. Roy, S. Shee and S. Kundu, Org. Biomol. Chem., 2016, 14, 10988 DOI: 10.1039/C6OB02010K

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