250598-98-2

Upstream product

• 100-39-0 benzyl bromide 
• 201863-39-0 (7S)-3,6-anhydro-1,2:4,5-di-O-isopropylidene-7-C-phenyl-D-glycero-D-manno-heptitol 
• 250598-96-0 (7S)-3,6-anhydro-1,2:4,5-di-O-isopropylidene-7-C-phenyl-7-O-(4-nitrobenzoyl)-D-glycero-D-manno-heptitol 
• 201863-41-4 (R)-[(3aR,4R,6R,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-phenyl-methanol 

Downstream Products

• 250599-00-9 (7S)-3,6-anhydro-7-O-benzyl-4,5-O-isopropylidene-1,2-bis-O-(methylsulfonyl)-7-C-phenyl-D-glycero-D-manno-heptitol 
• 250599-04-3 (7S)-3,6-anhydro-7-O-benzyl-2-deoxy-7-C-phenyl-D-altro-1,4-heptanolactone 
• 250599-01-0 (7S)-3,6-anhydro-7-O-benzyl-1,2-dideoxy-4,5-O-isopropylidene-7-C-phenyl-D-altro-hept-1-enitol 
• 250598-82-4 (7S)-3,6-anhydro-7-O-benzyl-1,2-dideoxy-7-C-phenyl-D-altro-hept-1-enitol 
• 250598-99-3 (7S)-3,6-anhydro-7-O-benzyl-1,2-O-isopropylidene-7-C-phenyl-D-glycero-D-manno-heptitol 

Relevant academic research and scientific papers

Synthesis and antitumor activity of goniofufurone analogues

Synthesis and antitumor activity of goniofufurone analogues 15, 16, 17, 33, and 46 is reported. Key step in the synthesis is Pd (II) mediated oxidative cyclisation of vinyl-(hydroxy) furans 18, 19 to the corresponding lactols 32, 43. Cytotoxicities of 15,