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Mild and General Protocol for Selective Deacetylation of Acetyl/Benzoyl-Protected Carbohydrates.
Abramov, Alexander A; Zinin, Alexander I; Kolotyrkina, Natalya G; Kononov, Leonid O; Shatskiy, Andrey; Kärkäs, Markus D; Stepanova, Elena V.
Afiliación
  • Abramov AA; Tomsk Polytechnic University, Lenin Avenue 30, 634050 Tomsk, Russia.
  • Zinin AI; Laboratory of Glycochemistry, N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russia.
  • Kolotyrkina NG; Laboratory of Glycochemistry, N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russia.
  • Kononov LO; Laboratory of Glycochemistry, N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russia.
  • Shatskiy A; Department of Chemistry, KTH Royal Institute of Technology, SE-100 44 Stockholm, Sweden.
  • Kärkäs MD; Department of Chemistry, KTH Royal Institute of Technology, SE-100 44 Stockholm, Sweden.
  • Stepanova EV; Tomsk Polytechnic University, Lenin Avenue 30, 634050 Tomsk, Russia.
J Org Chem ; 89(14): 10021-10026, 2024 Jul 19.
Article en En | MEDLINE | ID: mdl-38955329
ABSTRACT
Herein, we report a mild and general protocol for chemoselective deacetylation of mixed acetyl- and benzoyl-protected carbohydrates under mild acidic conditions. The protocol allows quick access to partially protected carbohydrates, which serve as versatile synthetic intermediates during the total synthesis of various mono- and oligosaccharide targets. The applicability of the developed protocol was successfully demonstrated on a range of carbohydrate substrates of various configurations and substitution patterns featuring functionalized aliphatic and aromatic aglycones. The protocol has shown excellent compatibility with the widely used O-anomeric protecting groups, prespacer aglycones, and thioglycoside glycosyl donors.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: Rusia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: Rusia
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