z-logo
Premium
Highly Efficient “Grafting onto” a Polypeptide Backbone Using Click Chemistry
Author(s) -
Engler Amanda C.,
Lee Hyungil,
Hammond Paula T.
Publication year - 2009
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200904070
Subject(s) - propargyl , click chemistry , ethylene glycol , grafting , polymerization , peg ratio , polymer chemistry , chemistry , ring opening polymerization , combinatorial chemistry , polymer science , organic chemistry , polymer , catalysis , finance , economics
“Clicked” into place : Densely grafted poly(γ‐propargyl‐ L ‐glutamate)‐g‐poly(ethylene glycol) polypeptides have been synthesized by combining ring‐opening polymerization of N ‐carboxyanhydrides with click chemistry. Various lengths of poly(ethylene glycol) (PEG) side chains (750 g mol −1 to 5000 g mol −1 ) were attached to a rigid α‐helical poly(γ‐propargyl‐ L ‐glutamate); extremely high grafting efficiencies of over 96 % were achieved.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom