Issue 1, 2009
From the journal:

New Journal of Chemistry

Dynamic covalent self-assembled macrocycles prepared from 2-formyl-aryl-boronic acids and 1,2-amino alcohols†

Ewan Galbraith,a   Andrew M. Kelly,a   John S. Fossey,a   Gabriele Kociok-Köhn,a   Matthew G. Davidson,a   Steven D. Bull*a  and  Tony D. James*a  

* Corresponding authors

a Department of Chemistry, University of Bath, Bath, UK
E-mail: S.D.Bull@bath.ac.uk, T.D.James@bath.ac.uk
Tel: +44 1225 383810

Abstract

Reaction of 2-formyl-aryl-boronic acids with 1,2-amino alcohols results in dynamic covalent self assembly to quantitatively afford tetracyclic macrocyclic Schiff base boracycles containing bridging boron–oxygen–boron functionality.

Graphical abstract: Dynamic covalent self-assembled macrocycles prepared from 2-formyl-aryl-boronic acids and 1,2-amino alcohols

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B815138E
Article type
Paper
Submitted
02 Sep 2008
Accepted
18 Sep 2008
First published
31 Oct 2008

New J. Chem., 2009,33, 181-185

Permissions

Request permissions

Dynamic covalent self-assembled macrocycles prepared from 2-formyl-aryl-boronic acids and 1,2-amino alcohols

E. Galbraith, A. M. Kelly, J. S. Fossey, G. Kociok-Köhn, M. G. Davidson, S. D. Bull and T. D. James, New J. Chem., 2009, 33, 181 DOI: 10.1039/B815138E

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