Cargando…
A stereoselective and flexible synthesis to access both enantiomers of N-acetylgalactosamine and peracetylated N-acetylidosamine
Synthetic approaches towards N-acetylgalactosamine (GalNAc) have been attracting considerable interest since this compound is known for its pivotal role in cell–cell interaction and receptor induced cell signaling. Herein, we present a synthetic route in which two of the four stereogenic centers pre...
Autores principales: | Riedl, Bettina, Schmid, Walther |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905266/ https://www.ncbi.nlm.nih.gov/pubmed/29719580 http://dx.doi.org/10.3762/bjoc.14.71 |
Ejemplares similares
-
Synthesis of both enantiomers of halitunal
por: Shimano, Kazunori, et al.
Publicado: (1996) -
Synthesis of Natural (−)-Antrocin and Its Enantiomer via Stereoselective Aldol Reaction
por: Angamuthu, Venkatachalam, et al.
Publicado: (2020) -
Liver-Targeted Delivery of Oligonucleotides with N-Acetylgalactosamine Conjugation
por: Cui, Hao, et al.
Publicado: (2021) -
The therapeutic prospects of N-acetylgalactosamine-siRNA conjugates
por: Zhang, Lei, et al.
Publicado: (2022) -
Peracetylated 4-Fluoro-glucosamine Reduces the Content and Repertoire of N- and O-Glycans without Direct Incorporation
por: Barthel, Steven R., et al.
Publicado: (2011)