Issue 32, 2019

A K+-promoted Diels–Alder reaction by using a self-assembled macrocyclic boronic ester containing two crown ether moieties

Abstract

A K+-promoted Diels–Alder reaction of 1,4,9,10-anthradiquinone with various dienes is achieved in the presence of a self-assembled macrocyclic boronic ester [2+2]crown containing two crown ether moieties. The reaction rate is remarkably accelerated (up to 206-fold) compared to that in the absence of the promoter. Furthermore, the reaction proceeds regioselectively to yield an internal adduct. The self-assembly protocol was also demonstrated.

Graphical abstract: A K+-promoted Diels–Alder reaction by using a self-assembled macrocyclic boronic ester containing two crown ether moieties

Supplementary files

Article information

Article type
Edge Article
Submitted
01 Apr 2019
Accepted
16 Jun 2019
First published
03 Jul 2019
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2019,10, 7627-7632

A K+-promoted Diels–Alder reaction by using a self-assembled macrocyclic boronic ester containing two crown ether moieties

K. Ono, M. Niibe and N. Iwasawa, Chem. Sci., 2019, 10, 7627 DOI: 10.1039/C9SC01597C

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.

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