Cargando…
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.
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017313/ https://www.ncbi.nlm.nih.gov/pubmed/29662042 http://dx.doi.org/10.3390/molecules23040914 |
_version_ | 1783334720781680640 |
---|---|
author | Céspedes Dávila, Maria F. Schneider, Jérémy P. Godard, Amélie Hazelard, Damien Compain, Philippe |
author_facet | Céspedes Dávila, Maria F. Schneider, Jérémy P. Godard, Amélie Hazelard, Damien Compain, Philippe |
author_sort | Céspedes Dávila, Maria F. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6017313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60173132018-11-13 One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides Céspedes Dávila, Maria F. Schneider, Jérémy P. Godard, Amélie Hazelard, Damien Compain, Philippe Molecules Communication 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. MDPI 2018-04-15 /pmc/articles/PMC6017313/ /pubmed/29662042 http://dx.doi.org/10.3390/molecules23040914 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Céspedes Dávila, Maria F. Schneider, Jérémy P. Godard, Amélie Hazelard, Damien Compain, Philippe One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides |
title | One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides |
title_full | One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides |
title_fullStr | One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides |
title_full_unstemmed | One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides |
title_short | One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides |
title_sort | one-pot, highly stereoselective synthesis of dithioacetal-α,α-diglycosides |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017313/ https://www.ncbi.nlm.nih.gov/pubmed/29662042 http://dx.doi.org/10.3390/molecules23040914 |
work_keys_str_mv | AT cespedesdavilamariaf onepothighlystereoselectivesynthesisofdithioacetalaadiglycosides AT schneiderjeremyp onepothighlystereoselectivesynthesisofdithioacetalaadiglycosides AT godardamelie onepothighlystereoselectivesynthesisofdithioacetalaadiglycosides AT hazelarddamien onepothighlystereoselectivesynthesisofdithioacetalaadiglycosides AT compainphilippe onepothighlystereoselectivesynthesisofdithioacetalaadiglycosides |