Issue 112, 2016

Enantioselective Diels–Alder reaction in the confined space of homochiral metal–organic frameworks

Abstract

A novel homochiral porous metal–organic framework (MOF) has been synthesized using (R)-2,2′-dihydroxy-1,1′-binaphthyl-4,4′-dibenzoic acid as the chiral ligand. This MOF acts as an effective heterogeneous catalyst for the enantioselective Diels–Alder reaction between isoprene and N-ethyl maleimide.

Graphical abstract: Enantioselective Diels–Alder reaction in the confined space of homochiral metal–organic frameworks

Supplementary files

Article information

Article type
Communication
Submitted
24 Sep 2016
Accepted
17 Nov 2016
First published
17 Nov 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2016,6, 111436-111439

Enantioselective Diels–Alder reaction in the confined space of homochiral metal–organic frameworks

K. Tanaka, S. Nagase, T. Anami, M. Wierzbicki and Z. Urbanczyk-Lipkowska, RSC Adv., 2016, 6, 111436 DOI: 10.1039/C6RA23740A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements