849619-42-7

Basic information

• Product Name: 1,6-anhydro-4-O-benzyl-2-O-[(S)-α-(ethoxycarbonyl)benzyl]-β-D-glucopyranose
• Synonyms: 1,6-anhydro-4-O-benzyl-2-O-[(S)-α-(ethoxycarbonyl)benzyl]-β-D-glucopyranose
• CAS NO: 849619-42-7
• Molecular Weight: 414.455
• Mol File: 849619-42-7.mol

Chemical Properties

• CAS DataBase Reference: 1,6-anhydro-4-O-benzyl-2-O-[(S)-α-(ethoxycarbonyl)benzyl]-β-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-anhydro-4-O-benzyl-2-O-[(S)-α-(ethoxycarbonyl)benzyl]-β-D-glucopyranose(849619-42-7)
• EPA Substance Registry System: 1,6-anhydro-4-O-benzyl-2-O-[(S)-α-(ethoxycarbonyl)benzyl]-β-D-glucopyranose(849619-42-7)

Safety Data

• Hazardous Substances Data: 849619-42-7(Hazardous Substances Data)

Upstream product

• 33208-47-8 4-O-benzyl-1,6:2,3-dianhydro-β-D-mannopyranose 
• 13704-09-1 (S)-(-)-ethyl mandelate 

Downstream Products

• 919081-72-4 1,6-anhydro-3-O-allyloxycarbonyl-4-O-benzyl-2-O-[(S)-ethoxycarbonylbenzyl]-β-D-glucopyranose 
• 865859-90-1 3,6-di-O-acetyl-4-O-benzyl-2-O-{(1S)-phenyl-2-(phenylsulfanyl)ethyl}-α-D-glucopyranosyl trichloroacetimidate 
• 865860-18-0 acetyl 3,6-di-O-acetyl-4-O-benzyl-2-O-{(S)-2-(phenylthiomethyl)benzyl}-α-D-glucopyranose 
• 865860-16-8 1,6-anhydro-4-O-benzyl-2-O-{(S)-2-(tosyloxymethyl)benzyl}-β-D-glucopyranose 
• 865860-17-9 1,6-anhydro-4-O-benzyl-2-O-{(S)-2-(phenylthiomethyl)benzyl}-β-D-glucopyranose 
• 919081-77-9 6-O-acetyl-3-O-allyloxycarbonyl-4-O-benzyl-2-O-[(S)-ethoxycarbonylbenzyl]-α-D-glucopyranosyl trichloroacetimidate 
• 919081-74-6 1,6-di-O-acetyl-3-O-allyloxycarbonyl-4-O-benzyl-2-O-[(S)-ethoxycarbonylbenzyl]-α-D-glucopyranose 
• 919081-63-3 1,6-anhydro-3-O-benzoyl-4-O-benzyl-2-O-[(S)-ethoxycarbonylbenzyl]-β-D-glucopyranose 
• 865860-15-7 1,6-anhydro-4-O-benzyl-2-O-{(S)-2-(hydroxymethyl)benzyl}-β-D-glucopyranose 

Relevant articles and documents

Stereoselective glycosylation reactions with chiral auxiliaries

Good neighbors: A chiral auxiliary is used for the first time to control the anomeric selectivity of glycosylation reactions. In this approach, upon treatment with an activator A+, neighboring-group participation pation of an (S)-ethoxycarbonyl

Stereoselective glycosylations using (R)- or (S)-(ethoxycarbonyl)benzyl chiral auxiliaries at C-2 of glycopyranosyl donors

The stereoselective introduction of a glycosidic bond presents the greatest challenge to complex oligosaccharide synthesis. Important developments such as automated polymer-supported oligosaccharide synthesis will not realize their full potential until th

A general strategy for stereoselective glycosylations

The principal challenge that the synthesis of oligosaccharides of biological importance presents is the development of a general approach for the stereoselective introduction of a glycosidic linkage. It is shown here that a (1S)-phenyl-2-(phenylsulfanyl)e