113410-07-4

Basic information

• Product Name: (2R,3S,4S,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran
• CAS NO: 113410-07-4
• Molecular Weight: 556.723
• Mol File: 113410-07-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3S,4S,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,4S,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran(113410-07-4)
• EPA Substance Registry System: (2R,3S,4S,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran(113410-07-4)

Safety Data

• Hazardous Substances Data: 113410-07-4(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 80040-79-5 3,4,6-tri-O-benzyl-D-galactal 
• 28715-70-0 methoxy-phenyl-sulfane 

Relevant articles and documents

Arylbis(arylthio)sulfonium Salts as Reagents for the Synthesis of 2-Deoxy-β-glycosides

The title sulfonium salts undergo electrophilic addition to glycals in the presence of alcohols to form principally β-glycosides.A substituent effect study has shown that the reagent with a p-tolylthio group is the most face-selective.By variation of the alcohol nucleophile, it has been shown that face selectivity is also dependent on the structure of the nucleophile.One instance of double diastereodifferentiation was uncovered when the racemic alcohol 23.5 was used in a reaction with tribenzyl glucal 22.1.The effect of glycal substitution on the face selectivity has led to the postulation of a heretofore unrecognized and still unexplained stereoelectronic effect.

SULFENATE ESTERS AS GLYCOSYL ACCEPTORS: A NOVEL APPROACH TO THE SYNTHESIS OF 2-DEOXYGLYCOSIDES

An approach to the synthesis of 2-deoxyglycosides from glycals was developed by use of Lewis acid mediated activation of benzenesulfenate esters.