55287-18-8

Upstream product

• 532-20-7 D-arabinofuranose 
• 108-24-7 acetic anhydride 
• 76-83-5 trityl chloride 
• 55726-00-6 (3S,4S,5R)-5-((trityloxy)methyl)tetrahydrofuran-2,3,4-triol 
• 28697-53-2 D-arabinopyranose 

Downstream Products

• 911455-31-7 1,3-dimethyl-7-β-D-xylofuranosyl-3,7-dihydro-purine-2,6-dione 
• 152772-76-4 1,2,3-tri-O-acetyl-5-O-p-toluenesulfonyl-D-arabinofuranosyl 
• 909885-30-9 7-α-D-Arabinofuranosyl theophylline 

Relevant academic research and scientific papers

Isoniazid Conjugates with D-Arabinofuranose

Glycoconjugates with isoniazid attached to the hydroxy group at the С5 atom of D-arabinofuranose via the spacers differing in length have been synthesized.

A simple synthesis of C-8 modified 2-keto-3-deoxy-d-manno-octulosonic acid (KDO) derivatives

This paper describes a simple and efficient method with which to prepare C-8 modified 2-keto-3-deoxy-D-manno-octu-losonic acid (KDO) derivatives from C-5 modified arabinose derivatives. Georg Thieme Verlag Stuttgart.

A facile synthesis of 5-thio-L-fucose and 5-thio-D-arabinose from D-arabinose

5-Thio-L-fucopyranose tetraacetate was synthesized in 11 steps from 5-O-trityl-D-arabinofuranose or D-arabinose diethyl dithioacetal by one-carbon elongation at C-5. Highly diastereoselective addition of MeLi in ether to a 1,2-O-isopropylidene-β-D-arabino

Synthesis of 1,5-dideoxy-1,5-imino-D-arabinitol (5-nor-L-fuco-1-deoxynojirimycin) and its application for the affinity purification and characterisation of α-L-fucosidase

The title, 1,5-dideoxy-1,5-imino-D-arabinitol (2), was synthesized in seven steps from D-arabinose with 5-azido-5-deoxy-D-arabinofuranose as key intermediate and 40percent overall yield.An affinity procedure employing the N-carboxypentyl derivative of 2 l