163580-29-8

Upstream product

• 14233-64-8 tri-O-benzyl-D-arabinolactone 
• 863871-31-2 (3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-2-trimethylsilanylethynyl-tetrahydro-furan-2-ol 
• 853260-31-8 ((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-ylethynyl)-trimethyl-silane 
• 163396-29-0 (3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-2-ethynyl-tetrahydro-furan-2-ol 

Downstream Products

• 853260-33-0 C₅₄H₅₄O₈ 

Relevant academic research and scientific papers

Synthesis of C-disaccharide analogues of the α-D-arabinofuranosyl- (1→5)-α-D-arabinofuranosyl motif of mycobacterial cell walls via alkynyl intermediates

Two C-glycosides related to the recurrent α-D-arabinofuranosyl- (1→5)-α-D-arabinofuranosyl structural motif of mycobacterial arabinan have been prepared by routes involving acetylenic intermediates.

A comparison of glucose- and glucosamine-related inhibitors: Probing the interaction of the 2-hydroxy group with retaining β-glucosidases

The inhibition of the β-glucosidases from sweet almonds and Caldocellum saccharolyticum at varying pH values by the glucosamine-related inhibitors 1- 7 has been compared to the inhibition by the known glucose analogues 8-14. The amino derivatives 3, 4, 6,

Synthesis of C-glycofuranosides by the stereoselective reduction of hemiacetals

Reaction of protected glycofuranolactones with organolithium reagents and reduction of the resultant hemiacetals with triethylsilane-boron trifluoride gives a stereocontrolled route to C-glycofuranosides, with hydride delivery occurring cis-to an adjacent