One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides

A one-step access to dithioacetal-α,α-diglycosides is reported. The synthetic strategy is based on the thioacetalization of aldehydes or ketones via highly stereoselective ring-opening of 1,6 anhydrosugars with bis(trimethylsilyl)sulfide.

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Bibliografske podrobnosti
izdano v:Molecules
Main Authors: Céspedes Dávila, Maria F., Schneider, Jérémy P., Godard, Amélie, Hazelard, Damien, Compain, Philippe
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2018
Teme:
Communication
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6017313/
https://ncbi.nlm.nih.gov/pubmed/29662042
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules23040914
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