20715-20-2

Upstream product

• 18439-42-4 ((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-phenyl-methanol 
• 18439-42-4 3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-L-ido-pentofuranose 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 65462-15-9 3-O-benzyl-1,2-O-isopropylidene-β-L-arabino-pentodialdo-1,4-furanose 

Downstream Products

• 18439-43-5 3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-D-gluco-pentafuranose 
• 18439-42-4 3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-L-ido-pentofuranose 
• 1234573-87-5 3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-D-ido-heptono-1,4-lactone 
• 1361026-55-2 C₂₀H₁₈O₄ 
• 1457973-59-9 C₂₀H₂₀O₄ 
• 899436-70-5 5-O-benzoyl-3-O-benzyl-1,2-isopropylidene-5-C-phenyl-α-D-gluco-pentofuranose 
• 144402-14-2 2-bromoacetyl-3,5-di-O-benzyl-5-C-phenyl-D-gluco-penta-1,4-lactone 
• 144402-15-3 6R,7R,8S-7-benzyloxy-1,5-dioxa-6-(R-benzyloxybenzyl)-2-oxobicyclo<3.3.0.>oct-3-ene 
• 144402-13-1 3,5-di-O-benzyl-5-C-phenyl-D-gluco-pento-1,4-lactone 
• 136778-39-7 (+)-goniofufurone 
• 144402-16-4 3,5-di-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-D-gluco-pentafuranose 
• 144402-17-5 3,5-di-O-benzyl-5-C-phenyl-α-D-gluco-pentofuranose 
• 917078-98-9 (4S,5R)-ethyl-5-((1R,2R,3R)-1,3-bis(benzyloxy)-3-phenyl-2-(triisopropylsilanyloxy)propyl)-2,2-dimethyl-1.3-dioxolane-4-carboxylate 
• 917079-00-6 methyl 2-((4R,5S)-5-((1R,2R,3R)-1,3-bis(benzyloxy)-3-phenyl-2-(triisopropylsilanyloxy)propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl)acetate 

Relevant academic research and scientific papers

Heteroannelated and 7-deoxygenated goniofufurone mimics with antitumour activity: Design, synthesis and preliminary SAR studies

Cytotoxic (+)-goniofufurone mimic such as benzoxepane 2 was preferentially formed after the treatment of 7-O-benzoyl-5-O-benzyl (+)-goniofufurone derivative 6 with titanium(IV) fluoride. However, the corresponding 7-epimer 5 (derivative of 7-epi-goniofufu

Asymmetric synthesis of (+)-cardiobutanolide

A formal total synthesis of (+)-cardiobutanolide has been accomplished from d-glucose, a readily available precursor.

Ethoxycarbonylmethylenetriphenylphosphorane in carbohydrate chemistry, part II: A short and efficient synthesis of (+)-goniofufurone

A concise approach to the synthesis of anti-tumor compound, goniofufurone is described starting from dialdo-xylose. The key step in our synthesis is the spontaneous lactonisation and Michael-ring closure accompanying the Wittig reaction of the title ylide

The total synthesis of goniofufurone

The total synthesis of natural (+)-Goniofufurone and related compounds from D-glucose is reported utilising a non-classical Wittig reaction. The factors governing the epimerisation of the tetronate 7 are also discussed.