1037290-72-4

Upstream product

• 16054-77-6 3,5-di-O-benzyl-D-xylofuranose 
• 86302-43-4 (tert-Butoxycarbonylmethylene)triphenylphosphorane 
• 1037290-71-3 tert-butyl (E)-5,7-di-O-benzyl-2,3-dideoxy-D-xylohept-2-enonate 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 1037290-75-7 5,7-di-O-benzyl-4,6-O-isopropylidene-1,2,3-tri-O-(methoxymethyl)-D-glycero-L-galactoheptitol 
• 1037290-76-8 5,7-di-O-benzyl-4,6-O-isopropylidene-1,2,3-tri-O-methoxymethyl-D-glycero-L-ido-heptitol 
• 1037290-96-2 5,7-di-O-benzyl-4,6-O-isopropylidene-D-glycero-L-galacto-heptitol 
• 1037291-05-6 5,7-di-O-benzyl-4,6-O-isopropylidene-D-glycero-L-ido-heptitol 
• 1305317-75-2 5,7-di-O-benzyl-4,6-O-isopropylidene-D-glycero-L-gulo-heptitol 
• 1305317-74-1 5,7-di-O-benzyl-4,6-O-isopropylidene-D-glycero-L-talo-heptitol 
• 1305317-73-0 C₂₄H₃₀O₆ 
• 1037290-74-6 (E)-5,7-di-O-benzyl-2,3-dideoxy-4,6-O-isopropylidene-D-xylo-hept-2-enitol 

Relevant academic research and scientific papers

Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor

Synthesis and evaluation of four diastereomers (9a, 9b, 9c and 9d) of kotalanol, a potent α-glucosidase inhibitor isolated from an Ayurvedic medicinal plant Salacia species, are described. Stereo-inversion at C-3′ and C-4′ of kotalanol (2) caused signific