1279230-33-9

Usage

Chemical Properties

White Crystals

Uses

A potential inhibitor of fucosyltransferase

Upstream product

• 55338-33-5 methyl 4,6-dideoxy-α-D-arabino-hexopyranoside 
• 102517-71-5 meso-2,6-octadiene-4,5-diolhexanediene-3,4-diol 
• 4486-59-3 dl-2,6-octadiene-4,5-diolhexanediene-3,4-diol 
• 28072-68-6 D-chalcose 
• 99838-53-6 2-O-Benzoyl-4,6-didesoxy-D-xylo-hexose 
• 99944-94-2 2,3-anhydro-5-O-benzyl-1,6,7,8-tetradeoxy-L-galacto-oct-6-enitol 
• 132867-78-8 1,2,3-tri-O-benzoyl-4,6-dideoxy-4-iodo-α-L-glucopyranose 
• 132867-76-6 1,2,3-tri-O-benzoyl-6-deoxy-α-L-galactopyranose 
• 10257-28-0 D-Galactose 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 56733-83-6 1,3-bis(N-benzyloxycarbonyl)-spectinomycin 
• 174278-21-8 Imidazole-1-carbothioic acid O-[(3aS,4S,6R,7R,7aS)-4-methoxy-2,2-dimethyl-6-(toluene-4-sulfonyloxymethyl)-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl] ester 
• 174278-22-9 methyl 4-deoxy-2,3-O-isoprpylidene-6-O-(p-tolylsulfonyl)-α-D-lyxo-hexopyranoside 

Downstream Products

• 91273-90-4 (E)-(4R,5R,7R)-4,5,7-Trihydroxy-oct-2-enoic acid 2-(toluene-4-sulfonyl)-ethyl ester 
• 91273-90-4 (E)-(4S,5S,7R)-4,5,7-Trihydroxy-oct-2-enoic acid 2-(toluene-4-sulfonyl)-ethyl ester 
• 148406-82-0 2-(p-tolylsulfonyl)ethyl (2E,4S,5S,7R)-7-hydroxy-4,5-isopropylidenedioxy-2-octenoate 
• 133463-56-6 2-(p-tolylsulfonyl)ethyl (10E,4S,5S,7R,13S)-13-t-butyldimethylsiloxy-4,5-isopropylidenedioxy-7-methyl-9-oxo-8-oxa-10-tetradecenoate 
• 133522-16-4 2-(p-tolylsulfonyl)ethyl (10E,4S,5S,7R,13R)-13-t-butyldimethylsiloxy-4,5-isopropylidenedioxy-7-methyl-9-oxo-8-oxa-10-tetradecenoate 
• 133463-55-5 2-(p-Toluenesulfonyl)ethyl (4S,5S,7R)-7-hydroxy-(4,5-dimethylmethylene)dioxyoctanoate 
• 91273-91-5 p-toluenesulfonylethyl (4R,5R,7R,2E)-7-hydroxy-4,5-dimethylmethylenedioxy-2-octenoate 
• 133522-15-3 2-(p-tolylsulfonyl)ethyl (10E,4R,5R,7R,13S)-13-t-butyldimethylsiloxy-4,5-isopropylidenedioxy-7-methyl-9-oxo-8-oxa-10-tetradecenoate 
• 133522-14-2 2-(p-Toluenesulfonyl)ethyl (4R,5R,7R)-7-hydroxy-(4,5-dimethylmethylene)dioxyoctanoate 

Relevant academic research and scientific papers

PREPARATION OF O-1 - C-6 AND O-7 - C-14 FRAGMENTS OF COLLETODIOL

(5S,2E)-5-Tetrahydropyranyloxy-2-hexenoic acid and p-toluenesulfonylethyl (4R,5R,7R,2E)-7-hydroxy-4,5-dimethylmethylenedioxy-2-octenoate were prepared from ethyl acetoacetate and D-glucose, respectively.

Synthesis and Structural Characteristics of all Mono- And Difluorinated 4,6-Dideoxy- d - Xylo-hexopyranoses

Protein-carbohydrate interactions are implicated in many biochemical/biological processes that are fundamental to life and to human health. Fluorinated carbohydrate analogues play an important role in the study of these interactions and find application a

Sugar-Pirating as an Enabling Platform for the Synthesis of 4,6-Dideoxyhexoses

An efficient divergent synthetic strategy that leverages the natural product spectinomycin to access uniquely functionalized monosaccharides is described. Stereoselective 2′- and 3′-reduction of key spectinomycin-derived intermediates enabled facile acces

Cytotoxic and HIF-1α inhibitory compounds from Crossosoma bigelovii

Cytotoxicity-guided fractionation of an organic solvent extract of the plant Crossosoma bigelovii led to the discovery of a new strophanthidin glycoside (1) and tw new 2-methylchromone glycosides (2 and 3). Also isolated were the known chromones eugenin a

Synthesis of 4-deoxy and 4-deoxy-4-halogeno derivatives of L-fucose as potential enzyme inhibitors

Methyl-2,3-di-O-benzoyl-6-deoxy-α-L-galactopyranoside (2) was converted into the 4-deoxy-4-iodo-α-L-gluco derivative 4 by triflate-mediated inversion.Catalytic reduction of 4 gave methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranoside (6) and subsequ

Formal total synthesis of grahamimycin A1

(S)-t-Butyldimethylsiloxy-2-hexenoic acid and its (R)-isomer were prepared from (S)- and (R)-3-hydroxybutanoic acid esters, respectively. Condensation of the both isomers with 2-(p-toluenesulfonyl)ethyl (4S,5S,7R)-7-hydroxy-4,5-dimethylmethylenedioxyoctan

SYNTHESIS OF 4,6-DIDEOXY-D- AND -L-HEXOSES FROM RACEMIC AND meso-DIPROPENYLGLYCOL

Rac- and meso-divinylglycols offer, via site-selective epoxidation, a versatile strategy for the synthesis of optically pure sugars.This is exemplified in this paper by the synthesis of 4,6-dideoxyhexoses.Starting from mono-O-benzyl di-(1-propenyl)glycol,