40838-18-4

Upstream product

• 58394-31-3 1,6-anhydro-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 
• 100-39-0 benzyl bromide 
• 161365-77-1 1,6-anhydro-2-chloro-β-D-erythro-hex-3-enopyranose 
• 100-51-6 benzyl alcohol 
• 112339-43-2 C₁₃H₁₆O₄ 
• 2873-29-2 D-glucal triacetate 
• 13265-84-4 D-glucal 
• 50705-28-7 1,6-anhydro-3,4-dideoxy-β-D-threo-hex-3-enopyranose 
• 102719-10-8 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose 
• 37112-31-5 levoglucosenone 
• 134441-71-7 (2S,4R)-1-boc-4-tert-butyldimethylsilylpyrrolidine-2-carbaldehyde 
• 251085-95-7 Trifluoro-methanesulfonic acid (1R,2S,5R)-2-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-en-4-yl ester 
• 58871-10-6 3,4-di-O-benzyl-D-glucal 
• 33208-47-8 4-O-benzyl-1,6:2,3-dianhydro-β-D-mannopyranose 

Downstream Products

• 148473-54-5 Acetic acid (1R,2R,3S,4R,5R)-2-benzyloxy-4-bromo-6,8-dioxa-bicyclo[3.2.1]oct-3-yl ester 
• 26540-44-3 4-O-benzyl-1,6:2,3-dianhydro-β-D-allopyranoside 
• 33208-47-8 4-O-benzyl-1,6:2,3-dianhydro-β-D-mannopyranose 
• 20183-84-0 1,6-anhydro-4-O-benzyl-β-D-allopyranose 
• 110046-93-0 1,6-anhydro-4-O-benzyl-2-bromo-2-deoxy-β-D-glucopyranose 

Relevant academic research and scientific papers

Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation

4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy deri

Convergent synthesis of (1→2)- and (1→4)-C-linked imino disaccharides

A convergent synthesis of (1→2)- and (1→4)-C-linked imino disaccharides was achieved by applying Nozaki-Kishi coupling of a hydroxyproline-derived carbaldehyde with isolevoglucosenone or levoglucosenone derived enol triflates.

Synthesis of 1,6-Anhydro-2-chloro-2,3,4-trideoxy-β-D-erythro-hex-3-enopyranose and its Stereospecific SN2' Substitution

The chlorination of 1,6-anhydro-3,4-dideoxy-β-D-threo-hex-3-enopyranose (2) with SOCl2 and pyridine gives predominantly 1,6-anhydro-2-chloro-β-D-erythro-hex-3-enopyranose (3).The chloride (3) takes place exclusively the suprafacial SN2' substit

Clay montmorillonite in carbohydrates : Use of 'claysil' as an efficient heterogenous catalyst for the intramolecular Ferrier reactions leading to 1,6-anhydro rare saccharides

Clay montmorillonite supported silver reagent - claysil - was prepared and advantageously used in the intramolecular Ferrier reaction of 6-hydroxy glycals 1a-9c. The unsaturated sugars 13a-21c so obtained were stereoselectively hydroxylated leading to the

Synthesis of 1,6-anhydro-2,3-dideoxy-β-D-erythro- and -threo-hex-2-enopyranose from 3,4-di-O-substituted glycals by a facile intramolecular Ferrier reaction

The 1,6-anhydro-2,3-dideoxy-β-D-erythro- 7-9 and -threo-hex-2-enopyranoses 10-12 are valuable synthons for the preparation of structurally diverse natural products. This paper reports on a new, general, and efficient route to their synthesis from 3,4-di-O