Literature DB >> 26360936

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

Kwang Soo Lee1, Jon R Parquette.   

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.

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Year:  2015        PMID: 26360936     DOI: 10.1039/c5cc06142c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  7 in total

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Journal:  Biomacromolecules       Date:  2021-04-12       Impact factor: 6.988

3.  Core-Substituted Naphthalenediimides: LUMO Levels Revisited, in Comparison with Preylenediimides with Sulfur Redox Switches in the Core.

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Journal:  Chem Sci       Date:  2017-03-17       Impact factor: 9.825

5.  Reorganization from Kinetically Stable Aggregation States to Thermodynamically Stable Nanotubes of BINOL-Derived Amphiphiles in Water.

Authors:  Filippo Tosi; Marc C A Stuart; Hans Smit; Jiawen Chen; Ben L Feringa
Journal:  Langmuir       Date:  2019-08-30       Impact factor: 3.882

6.  Threading carbon nanotubes through a self-assembled nanotube.

Authors:  Mingyang Ji; McKensie L Mason; David A Modarelli; Jon R Parquette
Journal:  Chem Sci       Date:  2019-08-01       Impact factor: 9.825

7.  Tandem reactions in self-sorted catalytic molecular hydrogels.

Authors:  Nishant Singh; Kai Zhang; César A Angulo-Pachón; Eduardo Mendes; Jan H van Esch; Beatriu Escuder
Journal:  Chem Sci       Date:  2016-05-09       Impact factor: 9.825

  7 in total

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