NoteStereospecific synthesis of β-d-allopyranosides by dihydroxylation of β-d-erythro-2,3-dideoxyhex-2-enopyranosides
-
Add time:09/03/2019 Source:sciencedirect.com
The synthesis of 4,6-O-benzylidene-β-d-erythro-2-3-dideoxyhex-2-enopyranosides and their osmium and ruthenium catalysed dihydroxylation reactions have been investigated. These reactions have been shown, for a range of monosaccharides and a disaccharide, to proceed stereospecifically to give β-d-allopyranosides in moderate to excellent yield.
We also recommend Trading Suppliers and Manufacturers of .beta.-D-Allopyranoside, methyl (cas 18469-06-2). Pls Click Website Link as below: cas 18469-06-2 suppliers
Prev:Molecular mechanism of action of Pelargonidin-3-O-glucoside, the main anthocyanin responsible for the anti-inflammatory effect of strawberry fruits
Next:Synthesis, pH-induced “on–off–on” luminescence switching, and partially intercalative DNA-binding and DNA photocleavage properties of an β-d-allopyranoside-grafted ruthenium(II) complex) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Cyanohydrins from methyl 6-deoxy-2,3-O-isopropylidene-α-l-lyxo-hexofuranosid-4-ulose via Bucherer–Bergs and Strecker reactions09/10/2019
- Alternansucrase acceptor reactions with methyl hexopyranosides09/09/2019
- Synthesis of 5-thio-d-allose and the methyl 5-thio-α- and -β-d-allopyranosides☆09/08/2019
- Synthesis of methyl 3,6-dibromo-3,6-dideoxy-β-d-allopyranoside and -glucopyranoside, and their interconversion in the presence of bromide ion09/07/2019
- Synthesis of the methyl 3-amino-3-deoxy-α- and β-d-allopyranosides and -allofuranosides09/06/2019
- NoteFrom methyl d-glucopyranoside to methyl d-allopyranoside via the Mitsunobu reaction09/05/2019
- Synthesis, pH-induced “on–off–on” luminescence switching, and partially intercalative DNA-binding and DNA photocleavage properties of an β-d-allopyranoside-grafted ruthenium(II) complex09/04/2019
-
Health and Chemical more >
-
Related Products
- Methyl 1-Benzyl-5-oxopyrrolidine-3-carboxylate
- Methyl (((methoxymethylphosphinothioyl)thio)acetyl)methylcarbamate
- Methyl (+)-(3R)-7-[4-(4-fluorophenyl)-6-isopropyl-2-(N-methyl-N-methanesulfonylamino)pyrimidin-5-yl]-3-hydroxy-5-oxo-(6E)-heptenoate
- Methyl (2-amino-5-methyl-1,3-thiazol-4-yl)acetate
- Methyl (2-chloromethyl)oxazole-4-carboxylate
- Methyl (2E)-3-(4-methylphenyl)propenoate
- Methyl (2E)-3-cyclohexylprop-2-enoate
- Methyl (2R)-2-[(tert-butoxycarbonyl)amino]-3-iodopropanoate
- Methyl (2R)-2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate
- Methyl (2R)-2-amino-2-cyclohexylethanoate hydrochloride


