A blog by two chemists working in chemistry and chemical biology
Wednesday, 6 March 2013
Synthetic polymers self-assembling into catalytic structures
Modern organic chemists have
access to a huge range of different chemical reactions and, these days, even
the most complicated natural product could probably be synthesised if somebody
wanted to. However, nature still does chemistry a hell of a lot better than
even the best organic chemist; enzymes allow even the simplest organism to
catalytically (and often asymmetrically) carry out organic reactions at room
temperature in an aqueous environment. Being able an enzyme’s characteristics artificially
would be, obviously, hugely advantageous. And there are a number of project on-going
particularly using supramolecular chemistry, dendrimers or polymers. Another method, one of the first in
a completely aqueous environment, has been described in a short communication
in Angerwandte by the Palmans group. It utilises a simple polymer functionalised with L-proline allowing it to
diastereoselectively catalyse an aldol reaction with cyclohexanone and
p-nitrobenzaldehyde.
Subscribe to:
Posts (Atom)