TY  - GEN
A1  - Doriti, Afroditi
A1  - Brosnan, Sarah M.
A1  - Weidner, Steffen M.
A1  - Schlaad, Helmut
T1  - Synthesis of polysarcosine from air and moisture stable N-phenoxycarbonyl-N-methylglycine assisted by tertiary amine base
N2  - Polysarcosine (Mn = 3650–20 000 g mol−1, Đ ∼ 1.1) was synthesized from the air and moisture stable N-phenoxycarbonyl-N-methylglycine. Polymerization was achieved by in situ transformation of the urethane precursor into the corresponding N-methylglycine-N-carboxyanhydride, when in the presence of a non-nucleophilic tertiary amine base and a primary amine initiator.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 255 
KW  - acids
KW  - activated urethane derivatives
KW  - carboxyanhydrides
KW  - copolymers
KW  - phosgene-free synthesis
KW  - polypeptides
KW  - ring-opening polymerization
Y1  - 2016
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-95852
SP  - 3067
EP  - 3070
ER  - 
TY  - JOUR
A1  - Doriti, Afroditi
A1  - Brosnan, Sarah M.
A1  - Weidner, Steffen M.
A1  - Schlaad, Helmut
T1  - Synthesis of polysarcosine from air and moisture stable N-phenoxycarbonyl-N-methylglycine assisted by tertiary amine base
JF  - Polymer Chemistry
N2  - Polysarcosine (M-n = 3650-20 000 g mol(-1), D similar to 1.1) was synthesized from the air and moisture stable N-phenoxycarbonyl-N-methylglycine. Polymerization was achieved by in situ transformation of the urethane precursor into the corresponding N-methylglycine-N-carboxyanhydride, when in the presence of a non-nucleophilic tertiary amine base and a primary amine initiator.
Y1  - 2016
U6  - https://doi.org/10.1039/c6py00221h
SN  - 1759-9954
SN  - 1759-9962
VL  - 7
SP  - 3067
EP  - 3070
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Doriti, Afroditi
A1  - Brosnan, Sarah M.
A1  - Weidner, Steffen M.
A1  - Schlaad, Helmut
T1  - Synthesis of polysarcosine from air and moisture stable N-phenoxycarbonyl-N-methylglycine assisted by tertiary amine base
JF  - Polymer Chemistry
N2  - Polysarcosine (Mn = 3650–20 000 g mol−1, Đ ∼ 1.1) was synthesized from the air and moisture stable N-phenoxycarbonyl-N-methylglycine. Polymerization was achieved by in situ transformation of the urethane precursor into the corresponding N-methylglycine-N-carboxyanhydride, when in the presence of a non-nucleophilic tertiary amine base and a primary amine initiator.
KW  - ring-opening polymerization
KW  - activated urethane derivatives
KW  - phosgene-free synthesis
KW  - carboxyanhydrides
KW  - polypeptides
KW  - acids
KW  - copolymers
Y1  - 2016
U6  - https://doi.org/10.1039/C6PY00221H
SN  - 1759-9954
SN  - 1759-9962
VL  - 7
SP  - 3067
EP  - 3070
PB  - RSC Publ.
CY  - Cambridge
ER  -