Utilisation d'ylides du phosphore non stabilisés en chimie des sucres. V. Sucres ramifiés dérivés du méthyl α‐D‐lyxo‐hexopyrannosul‐4‐oside. Communication préliminaire
- 1 January 1970
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 53 (2) , 364-368
- https://doi.org/10.1002/hlca.19700530217
Abstract
Cis and trans‐methyl‐4‐deoxy‐2, 3‐O‐isopropylidene‐6‐O‐methyl‐4‐methylthio‐methylene‐α‐D‐lyxo‐hexopyra‐nosides are prepared by a Wittig reaction. Methods are described for the determination of the configuration of the geometrical isomers whose Raney‐Nickel reduction leads to derivatives of 4‐deoxy‐4‐methyl‐hexoses of the D‐manno and D‐talo series.Keywords
This publication has 5 references indexed in Scilit:
- Utilisation d'ylides du phosphore non stabilisés en chimie des sucres. IV. Nouveaux exemples de sucres méthylthiovinyliques terminaux. Communication préliminaireHelvetica Chimica Acta, 1970
- Utilisation d'ylides du phosphore non stabilisés en chimie des sucres. II. Action du méthylthiométhylène‐triphénylphosphorane sur les aldéhydo‐surcesHelvetica Chimica Acta, 1969
- The relative abilities of methoxy and methylthio substituents to stabilize double bondsThe Journal of Organic Chemistry, 1967
- Regel zur Abschätzung der chemischen Verschiebung von Protonen an einer DoppelbindungHelvetica Chimica Acta, 1966
- The Action of Triphenylchloromethane on α-Methyl-D-mannopyranosideJournal of the American Chemical Society, 1939