110920-93-9

Upstream product

• 2031-48-3 Benzaldehyde dipent-4-enyl acetal 
• 110920-92-8 (3aR,5R,6S,6aR)-5-((R)-2-(tert-butyldiphenylsilyloxy)-1-hydroxyethyl)-2,2-dimethyltetrahydrofuro(3,2-d)(1,3)dioxol-6-ol 
• 100-52-7 benzaldehyde 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 
• 774-48-1 (diethoxymethyl)benzene 
• 110920-92-8 (3aR,5R,6S,6aR)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 1125-88-8 benzaldehyde dimethyl acetal 

Downstream Products

• 141242-30-0 3-O-benzoyl-5-bromo-5-deoxy-1,2-O-isopropylidene-β-L-idofuranose 
• 141242-37-7 5-Azido-6-O-benzoyl-1,3,5-dideoxy-3-fluoro-1,2-O-isopropylidene-α-D-glucofuranose 
• 141242-34-4 3,6-di-O-benzoyl-5-deoxy-1,2-O-isopropylidene-β-L-threo-hex-4-enofuranose 
• 108782-72-5 3,6-di-O-benzoyl-5-bromo-5-deoxy-1,2-O-isopropylidene-β-L-idofuranose 
• 141242-35-5 5-azido-6-O-tert-butyldiphenylsilyl-3,5-dideoxy-3-fluoro-1,2-O-isopropylidene-α-D-glucofuranose 
• 141242-29-7 5-azido-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 141242-33-3 3-O-benzoyl-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-β-L-threo-hex-4-enofuranose 
• 141242-28-6 5-bromo-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-β-L-talofuranose 
• 140451-82-7 3-O-benzoyl-5-bromo-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 140451-85-0 5-azido-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 
• 140451-84-9 5-Azido-3-O-benzoyl-5-deoxy-1,2-O-isopropylidene-6-O-tert-butyldiphenylsilyl-α-D-allofuranose 
• 110920-92-8 (3aR,5R,6S,6aR)-5-((R)-2-(tert-butyldiphenylsilyloxy)-1-hydroxyethyl)-2,2-dimethyltetrahydrofuro(3,2-d)(1,3)dioxol-6-ol 
• 111056-67-8 3,5-O-(S)-benzylidene-6-deoxy-6-iodo-1,2-O-isopropylidene-α-D-glucofuranose 
• 111003-74-8 3,5-O-(R)-benzylidene-6-deoxy-6-iodo-1,2-O-isopropylidene-α-D-glucofuranose 

Relevant academic research and scientific papers

Synthesis and reactions of 3-C-branched-chain analogues of 3,6-anhydrodeoxynojirimycin

The syntheses of 3,6-anhydro-1-deoxy-3-C-ethoxycarbonylmethyl- (4) and 3-C-(2-hydroxyethyl)nojirimycin (5) from 5-azido-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-α-D- glucofuranose (8) are described. The key intermediate is 5-azido-6-O-tert

Dipent-4-enyl Acetals as Acetalization Agents

Dipent-4-enyl acetals, which are conveniently prepared by treating ketones or aldehydes with pent-4-enyl alcohol under standard conditions, readily acetalize diols in acetonitrile solvent, and although neutral promoters such as N-halogenosuccinimides and

Synthesis, reactions, and crystal structure of 5-azido-6-O-benzoyl-3,5-dideoxy-3-fluoro-1,2-O-isopropylidene-α-D-gluc ofuranose

5-Bromo-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-β-L-t alofuranose (7) was obtained by treatment of 3,5-O-benzylidene-6-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-α-D -glucofuranose (3) with N-bromosuccinimide followed by Zemplen O-dea

An Improvement in the Preparation of Some Carbohydrate Benzylidene Acetals

Carbohydrate benzylidene and p-methoxybenzylidene acetals are easily prepared by treatment of various sugar derivatives with either benzaldehyde diethyl acetal or p-methoxybenzaldehyde diethyl acetal, respectively, in refluxing chloroform containing camph

SPECIFIC SYNTHESIS AND STEREOCHEMICAL ASSIGNMENT OF THE DIASTEREOMERIC 3,5-O-BENZYLIDENE-1,2-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE ISOMERS

Pyridinium tosylate-catalysed acetal exchange between benzaldehyde dimethyl acetal and 6-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-α-D-glucofuranose was investigated as an alternative to the original procedure of Brigl and Gruener (condensation of