79774-58-6

Upstream product

• 79813-89-1 benzyl 4,6-O-benzylidene-2-deoxy-α-D-arabino-hexopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 50615-76-4 benzyl 2-deoxy-α-D-arabino-hexopyranoside 
• 79774-57-5 benzyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-arabino-hexopyranoside 

Downstream Products

• 79774-61-1 benzyl 3,4-di-O-benzyl-2,6,7-trideoxy-7-diethoxyphosphinoyl-α-D-arabino-hept-6-trans-enopyranoside 
• 79774-69-9 benzyl 3,4-di-O-benzyl-2,6-dideoxy-6-diethoxyphosphinoyl-α-D-arabino-hexopyranoside 
• 79774-60-0 benzyl 3,4-di-O-benzyl-2-deoxy-α-D-arabino-hexodialdo-1,5-pyranoside 
• 79774-68-8 benzyl 3,4-di-O-benzyl-6-bromo-2,6-dideoxy-α-D-arabino-hexopyranoside 

Relevant academic research and scientific papers

Synthesis of cyclophospho-glucoses and glucitols

The syntheses of cyclophosphodiesters of 5-C-(hydroxymethyl)-hexoses and hexitols and of 6-C-(hydroxymethyl)-hexoses are reported, along with that of 6-deoxy-gluco-heptose 7-phosphate. These compounds proved to be reasonable substrate mimics and show inhibitory activity against human d-myo-inositol 3-phosphate synthase.

SYNTHESIS OF PHOSPHONO ANALOGUES OF 3-DEOXY-D-arabino-HEPT-2-ULOSONIC ACID 7-PHOSPHATE

3,7,8-Trideoxy-8-phosphono-D-arabino-octulosonic acid and 7,8-dideoxy-8-phosphono-D-gluco-octulosonic acid were synthesised in six steps from known, protected derivatives of 2-deoxy-D-arabino-hexose and D-glucose.The protected 6-aldehydo-hexodialdoses wer