Cargando…
Allyl Cyanate/Isocyanate Rearrangement in Glycals: Stereoselective Synthesis of 1-Amino and Diamino Sugar Derivatives
[Image: see text] The [3,3]-sigmatropic allyl cyanate/isocyanate rearrangement of glycals in the presence of O-, N-, and C-nucleophiles afforded β-N-glucosyl and galactosyl carbamates, ureas, and amides in good yields. The unsaturated products were elaborated to N-glycosides by dihydroxylation, to 1...
Autores principales: | Mirabella, Stefania, Petrucci, Giulia, Faggi, Cristina, Matassini, Camilla, Cardona, Francesca, Goti, Andrea |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735751/ https://www.ncbi.nlm.nih.gov/pubmed/33147974 http://dx.doi.org/10.1021/acs.orglett.0c03438 |
Ejemplares similares
-
Stereoselective
Synthesis of Heavily Hydroxylated
Azepane Iminosugars via Osmium-Catalyzed Tethered Aminohydroxylation
por: Martínez-Bailén, Macarena, et al.
Publicado: (2023) -
Stereoselective Synthesis of 2-Deoxythiosugars from Glycals
por: You, Xueying, et al.
Publicado: (2022) -
Palladium‐Catalyzed Direct Stereoselective Synthesis of Deoxyglycosides from Glycals
por: Sau, Abhijit, et al.
Publicado: (2017) -
Gold(I)-Catalyzed
Direct Stereoselective Synthesis
of Deoxyglycosides from Glycals
por: Palo-Nieto, Carlos, et al.
Publicado: (2017) -
Piperidine Azasugars
Bearing Lipophilic Chains: Stereoselective
Synthesis and Biological Activity as Inhibitors of Glucocerebrosidase
(GCase)
por: Clemente, Francesca, et al.
Publicado: (2021)