Aziridine Ring Opening as Regio- and Stereoselective Access to C-Glycosyl-Aminoethyl Sulfide Derivatives

A short synthetic route to stereoselective access to C-glycosyl-aminoethyl sulfide derivatives has been developed through the reaction of tributhyltin derivatives of glycals with aziridinecarboaldehyde and the regioselective ring opening of a chiral aziridine with thiophenol. The absolute configurat...

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Detalles Bibliográficos
Autores principales: Tracz, Aleksandra, Malinowska, Martyna, Leśniak, Stanisław, Zawisza, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952378/
https://www.ncbi.nlm.nih.gov/pubmed/35335129
http://dx.doi.org/10.3390/molecules27061764

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952378/
https://www.ncbi.nlm.nih.gov/pubmed/35335129
http://dx.doi.org/10.3390/molecules27061764

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