162466-16-2

Upstream product

• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 162466-15-1 (2S,3R)-2,3-isopropylidenyloxy-3-phenylpropanyl tert-butyldiphenylsilyl ether 
• 162466-13-9 (2S,3R)-2-hydroxy-3-acetoxyl-3-phenylpropanyl tert-butyldiphenylsilyl ether 
• 162466-14-0 (2S,3R)-2,3-dihydroxy-3-phenylpropanyl tert-butyldiphenylsilyl ether 
• 162600-01-3 (1S,2R,3R)-1-(2-furyl)-2,3-isopropylidenyloxy-3-phenyl-1-propanol 
• 163748-92-3 Acetic acid (2S,3R)-2,3-dihydroxy-3-phenyl-propyl ester 
• 162466-12-8 (2S,3R)-3-acetoxyl-3-phenyl-1,2-propanediol 
• 162600-00-2 ((4S,5R)-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-yl)methanol 
• 21915-53-7 (2R,3S)-(3-phenyloxiran-2-yl)methanol 
• 130718-77-3 (4R,5R)-cis-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-carbaldehyde 

Downstream Products

• 96405-62-8 (5S,6R)-6-[(1S,2R)-1-(benzyloxy)-1,2-dihydroxy-2-phenylethyl]-5-hydroxy-5,6-dihydro-2H-pyran-2-one 
• 136778-39-7 (+)-goniofufurone 
• 144429-71-0 (6R,7R,8R)-goniodiol-8-monoacetate 
• 129578-08-1 8-O-acetylgoniotriol 
• 151830-90-9 4,6-O-Isopropylidene-7-C-phenyl-D-gluco-hept-2-enono-δ-lactone 
• 163630-04-4 Acetic acid (2R,3S)-2-((4R,5R)-2,2-dimethyl-5-phenyl-[1,3]dioxolan-4-yl)-6-oxo-3,6-dihydro-2H-pyran-3-yl ester 

Relevant academic research and scientific papers

Asymmetric Total Synthesis of (+)-Goniotriol and (+)-Goniofufurone

Thr Enantioselective synthesis of two antitumor styryl lactones, (+)-goniotriol and (+)-goniofufurone, have been completed starting from cinnamyl alcohol in ten and eleven steps with an overall yield of 21percent and 12percent, respectively.

Total synthesis of the natural goniodiol-8-monoacetate from cinnamyl alcohol

The first total synthesis of goniodiol-8-monoacetate, using the Sharpless asymmetric epoxidation starting from cinnamyl alcohol in twelve steps with an overall yield of 7%, is achieved.