TY  - JOUR
A1  - Secker, Christian
A1  - Robinson, Joshua W.
A1  - Schlaad, Helmut
T1  - Alkyne-X modification of polypeptoids
JF  - European polymer journal
N2  - Poly(N-propargyl glycine) (PNPG) can be readily prepared by ring-opening polymerization of N-propargyl glycine N-carboxyanhydride (NCA) and modified using various addition reactions such as copper catalyzed [3+2] cycloaddition of azide, radical (photo-)addition of thiol, nucleophilic addition of ethylene oxide, and thermal induced cross-linking. It is demonstrated that PNPG can serve as a modular platform to produce a bibliography of novel functional polypeptoid or pseudopeptide materials, including polypeptoid ionic liquids and graft copolymers.
KW  - Polypeptoid
KW  - NCA
KW  - Post-polymerization modification
KW  - Click chemistry
Y1  - 2015
U6  - https://doi.org/10.1016/j.eurpolymj.2014.08.028
SN  - 0014-3057
SN  - 1873-1945
VL  - 62
SP  - 394
EP  - 399
PB  - Elsevier
CY  - Oxford
ER  - 
TY  - JOUR
A1  - Brosnan, Sarah M.
A1  - Schlaad, Helmut
T1  - Modification of polypeptide materials by Thiol-X chemistry
JF  - Polymer : the international journal for the science and technology of polymers
N2  - Thiol-X chemistry has proven to be a valuable toolbox for modification of peptides, proteins, monomers, and polymers. Recently, this has become especially true for the modification of polypeptides (monomers or polymers), which has resulted in a plethora of novel polymers and materials. With this in mind, this highlight focuses on the recent literature concerning the modification of polypeptides by the use of thiol-X chemistry, in particular to synthetic polypeptides either at the monomer or polymer stage modified by thiol-ene, -Michael addition, and -yne chemistries. (C) 2014 Published by Elsevier Ltd.
KW  - Polypeptide
KW  - Thiol-X
KW  - Click chemistry
Y1  - 2014
U6  - https://doi.org/10.1016/j.polymer.2014.08.067
SN  - 0032-3861
SN  - 1873-2291
VL  - 55
IS  - 22
SP  - 5511
EP  - 5516
PB  - Elsevier
CY  - Oxford
ER  -