956317-01-4

Upstream product

• 3067-56-9 D-glucurono-3,6-lactone acetonide 
• 170872-96-5 (+)-1,2-O-Isopropylidene-5-O-(phenoxythiocarbonyl)-α-D-glucurono-6,3-lactone 
• 111651-70-8 (3aR,6R,6aS)-6-Benzyloxy-5-methoxy-tetrahydro-furo[3,2-b]furan-2-one 
• 111651-69-5 (3aR,6R,6aR)-6-Hydroxy-5-methoxy-tetrahydro-furo[3,2-b]furan-2-one 
• 15354-75-3 3-O-benzyl-1,2-O-cyclohexylidene-α-D-xylo-pentodialdo-1,4-furanose 
• 956317-00-3 5-O-benzoyl-3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-α-D-gluco-pentofuranose 
• 138847-58-2 3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-α-D-gluco-pentofuranose 
• 138847-59-3 3-O-benzyl-1,2-O-cyclohexylidene-5-C-phenyl-β-L-ido-pentofuranose 
• 2033-24-1 cycl-isopropylidene malonate 

Downstream Products

• 136778-39-7 (+)-goniofufurone 
• 1361026-52-9 C₂₀H₁₉ClO₄ 
• 1361026-60-9 C₂₀H₁₉BrO₄ 
• 1361026-58-5 3,6-anhydro-2,7-dideoxy-7-C-phenyl-7-bromo-D-glycero-D-ido-heptono-1,4-lactone 
• 1361026-59-6 3,6-anhydro-2,7-dideoxy-7-C-phenyl-7-bromo-L-glycero-D-ido-heptono-1,4-lactone 
• 1361026-53-0 3,6-anhydro-2,7-dideoxy-7-C-phenyl-7-chloro-D-glycero-D-ido-heptono-1,4-lactone 
• 1361026-54-1 3,6-anhydro-2,7-dideoxy-7-C-phenyl-7-chloro-L-glycero-D-ido-heptono-1,4-lactone 

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

Stereospecific α-alkoxystannane couplings with acyl chlorides: Total synthesis of (+)-goniofufurone

Stereospecific C-glycoside formation via Pd/Cu mediated coupling of PhCOCl with cyclic α-alkoxystannane 6, derived from D-glucurono-6,3-lactone, was the key transformation in a concise total synthesis of the anticancer agent (+)-goniofufurone.