Cargando…
1,1,3,3-Tetramethylguanidine-Mediated Zwitterionic Ring-Opening Polymerization of Sarcosine-Derived N-Thiocarboxyanhydride toward Well-Defined Polysarcosine
[Image: see text] Zwitterionic ring-opening polymerization (ZROP) of sarcosine-derived N-thiocarboxyanhydrides (Me-NNTAs) can be induced by using 1,1,3,3-tetramethylguanidine (TMG) initiators in CH(2)Cl(2) at 25 °C, rapidly producing well-defined polysarcosine polymers with controlled molecular weig...
Autores principales: | Siefker, David, Chan, Brandon A., Zhang, Meng, Nho, Ju-Woo, Zhang, Donghui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011146/ https://www.ncbi.nlm.nih.gov/pubmed/35444344 http://dx.doi.org/10.1021/acs.macromol.1c02472 |
Ejemplares similares
-
2-Acetyl-1,1,3,3-tetramethylguanidine
por: Tiritiris, Ioannis
Publicado: (2012) -
2-[2-(Benzylsulfanyl)phenyl]-1,1,3,3-tetramethylguanidine
por: Neuba, Adam, et al.
Publicado: (2011) -
Development of a rapid GC-FID method to simultaneously determine triethylamine, diisopropylamine, and 1,1,3,3-tetramethylguanidine residues in an active pharmaceutical ingredient
por: Shou, Minshan, et al.
Publicado: (2021) -
Efficient Shielding of Polyplexes Using Heterotelechelic Polysarcosines
por: Klein, Philipp Michael, et al.
Publicado: (2018) -
Direct N-substituted N-thiocarboxyanhydride polymerization towards polypeptoids bearing unprotected carboxyl groups
por: Zheng, Botuo, et al.
Publicado: (2020)