Cargando…
Enzymatic separation of epimeric 4-C-hydroxymethylated furanosugars: Synthesis of bicyclic nucleosides
Conversion of D-glucose to 4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-ribofuranose, which is a key precursor for the synthesis of different types of bicyclic/spiro nucleosides, led to the formation of an inseparable 1:1 mixture of the desired product and 4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xy...
Autores principales: | Rana, Neha, Kumar, Manish, Khatri, Vinod, Maity, Jyotirmoy, Prasad, Ashok K |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647706/ https://www.ncbi.nlm.nih.gov/pubmed/29062429 http://dx.doi.org/10.3762/bjoc.13.205 |
Ejemplares similares
-
NAD(+)‐Dependent Enzymatic Route for the Epimerization of Hydroxysteroids
por: Tonin, Fabio, et al.
Publicado: (2018) -
Chemical and chemoenzymatic routes to bridged homoarabinofuranosylpyrimidines: Bicyclic AZT analogues
por: Kumar, Sandeep, et al.
Publicado: (2022) -
Double-headed nucleosides: Synthesis and applications
por: Verma, Vineet, et al.
Publicado: (2021) -
Analogues of Muraymycin Nucleoside Antibiotics with Epimeric Uridine-Derived Core Structures
por: Spork, Anatol P., et al.
Publicado: (2018) -
Synthesis of dinucleoside acylphosphonites by phosphonodiamidite chemistry and investigation of phosphorus epimerization
por: Hersh, William H
Publicado: (2015)