15354-75-3

Upstream product

• 13322-89-9 3-O-Benzyl-1,2-O-cyclohexylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 23397-76-4 1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose 
• 13322-88-8 3-O-benzyl-1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose 
• 645403-02-7 3-O-benzyl-1,2-O-cyclohexilidene-α-D-xylofuranose 
• 76800-60-7 5-O-benzoate-1,2-O-cyclohexylidene-α-D-xylofuranose 
• 645402-97-7 5-O-benzoyl-3-O-benzyl-1,2-O-cyclohexylidene-α-D-xylofuranose 

Downstream Products

• 58990-22-0 1,2-O-Cyclohexylidene-3-O-benzyl-6-deoxy-6-C-(2-pyridyl)-α-D-xylohexo-1,4-furanose 
• 58990-23-1 (5Ξ)-5-benzothiazol-2-yl-O³-benzyl-O¹,O²-cyclohexane-1,1-diyl-α-D-xylofuranose 
• 22169-86-4 2-((3'aR)-6'c-benzyloxy-(3'ar,6'ac)-tetrahydro-spiro[cyclohexane-1,2'-furo[2,3-d][1,3]dioxol]-5'c-yl)-5-methyl-quinoline-4-carboxylic acid 
• 22169-84-2 2-((3'aR)-6'c-benzyloxy-(3'ar,6'ac)-tetrahydro-spiro[cyclohexane-1,2'-furo[2,3-d][1,3]dioxol]-5'c-yl)-5-bromo-quinoline-4-carboxylic acid 
• 645403-03-8 methyl (Z)-3-O-benzyl-5,6-dideoxy-1,2-O-cyclohexylidene-α-D-xylo-hept-5-enofuranuronate 
• 1083324-84-8 methyl (E)-3-O-benzyl-5,6-dideoxy-1,2-O-cyclohexylidene-α-D-xylo-hept-5-enofuranuronate 
• 645403-08-3 C₂₉H₄₄O₄ 
• 138847-59-3 3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-β-L-ido-pentofuranose 
• 138847-58-2 3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-α-D-gluco-pentofuranose 

Relevant academic research and scientific papers

Enantiodivergent synthesis of cytotoxic styryl lactones from d-xylose. The first total synthesis of (+)- and (-)-crassalactone C

Enantiodivergent total syntheses of both (+)- and (-)-enantiomers of goniofufurone, 7-epi-goniofufurone and crassalactone C have been accomplished starting from d-xylose. The key steps of the synthesis of 7-epi-(+)-goniofufurone were a stereo-selective ad

Synthesis and antiproliferative activity of unnatural enantiomers of 7-epi-goniofufurone and crassalactone C

A facile synthesis of 7-epi-(-)-goniofufurone as well as the first synthesis of (-)-crassalactone C was achieved starting from d-xylose. A comparison of their in vitro antitumour activities with those observed for the corresponding naturally occurring enantiomers was provided.

Enantiodivergent synthesis of muricatacin related lactones from d-xylose based on the latent symmetry concept: preparation of two?novel cytotoxic (+)- and (-)-muricatacin 7-oxa analogs

Enantiodivergent formal synthesis of (+)- and (-)-muricatacins from d-xylose has been accomplished through utilization of the?latent plane of symmetry present in the starting monosaccharide. This approach was extended to the preparation of two novel (+)-

[3+2] Cycloaddition reactions: A simple entry to the 1-aza-2-oxo-3,4,5,6- tetrahydroxybicyclo[3.3.0]octane ring system

The [3+2] intramolecular nitrone cycloaddition (INC) reaction on appropriately designed olefinic nitrones derived from D-glucose, having the nitrone at C-1 and α,β-unsaturated ester functionalities at C-5 of the sugar backbone, afforded the isoxazolidine

Enantiopure hydroxylactones from D-xylose. A novel approach to the enantiodivergent synthesis of (+)- and (-)-muricatacin suitable for the preparation of 7-oxa analogues

A new route towards enantiopure hydroxylactones 3 and ent-3, the final chiral precursors in an enantiodivergent synthesis of (+)- and (-)-muricatacin, has been developed starting from D-xylose.