Boron trifluoride etherate as an effective reagent for the stereoselective one-pot conversion of acetylated 2-trimethylsilylethyl glycosides into sugar 1,2-trans-acetates-Reference-Cited by-同舟云学术

Boron trifluoride etherate as an effective reagent for the stereoselective one-pot conversion of acetylated 2-trimethylsilylethyl glycosides into sugar 1,2-trans-acetates

Published:1986-01 Issue:6 Volume:27 Page:753-756
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Jansson Karl,Frejd Torbjörn,Kihlberg Jan,Magnusson Göran

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. 1,2-Orthoacetate intermediates in silver trifluoromethanesulphonate promoted Koenigs–Knorr synthesis of disaccharide glycosides

2. The snythesis of disaccharides by the ferric chloride-catalyzed coupling of 2-acylamido-2-deoxy-β-D-glucopyranose 1-acetates to protect sugar acceptors

3. BF3--Etherate Induced Formation of 2,2,2-Trichloroethyl Glycopyranosides. Selective Visualization of Carbohydrate Derivatives on TLC Plates.

4. Boron trifluoride etherate-induced glycosidation: formation of alkyl glycosides and thioglycosides of 2-deoxy-2-phthalimidoglycopyranoses

5. Lewissäure-katalysierte synthesen von di- und trisaccharid-sequenzen der O- und N-glycoproteine. Anwendung von trimethylsilyltrifluoromethanesulfonat

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