Issue 86, 2015

A self-assembled nanotube for the direct aldol reaction in water

Abstract

Nanotubes formed by the aqueous assembly of a proline–lysine dipeptide (1) were used to create the hydrophobic microenvironments required to catalyze the aldol reaction in water. The self-assembly process occurred most efficiently in the presence of the substrates, producing an array of homogeneous nanotubes under the reaction conditions. The nanotubes formed by dipeptide 1 served as an efficient catalyst for the aldol reaction that functioned at low loading levels and provided good to excellent conversions. The catalytic activity of 1 was minimal under conditions that dissociated the nanotube into soluble monomers.

Graphical abstract: A self-assembled nanotube for the direct aldol reaction in water

Supplementary files

Article information

Article type
Communication
Submitted
22 Jul 2015
Accepted
03 Sep 2015
First published
03 Sep 2015

Chem. Commun., 2015,51, 15653-15656

Author version available

A self-assembled nanotube for the direct aldol reaction in water

K. S. Lee and J. R. Parquette, Chem. Commun., 2015, 51, 15653 DOI: 10.1039/C5CC06142C

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