138847-58-2

Upstream product

• 15354-75-3 3-O-benzyl-1,2-O-cyclohexylidene-α-D-xylo-pentodialdo-1,4-furanose 
• 1204408-00-3 3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-α-D-xylo-pentofuran-5-ulose 
• 100-58-3 phenylmagnesium bromide 
• 138847-59-3 3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-β-L-ido-pentofuranose 

Downstream Products

• 136778-39-7 (+)-goniofufurone 
• 956317-01-4 3,6-anhydro-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone 
• 1234573-62-6 3,5-di-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

Divergent synthesis of cytotoxic styryl lactones from D-xylose. The first total synthesis of (+)-crassalactone C

A new divergent approach to (+)-goniofufurone (1) and 7-epi-(+)- goniofufurone (2), as well as the first total synthesis of crassalactone C (3), has been achieved starting from o-xylose. In a preliminary bioassay, all three natural products 1, 2, and 3 sh