844868-75-3

Upstream product

• 844868-73-1 methoxy-phenyl-acetic acid 6-[2-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenyl]-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-hex-4-enyl ester 
• 844868-72-0 [3-(3'7'-dimethyl-2-octen-6'S,7'-diol)-4-(tert-butyldimethyl-siloxy)-5-methoxy-benzyloxy]-tert-butyldimethylsilane 
• 474970-89-3 [4-(tert-butyldimethylsiloxy)-5-methoxy-3-(3',7'-dimethyl-2',6'-octadienyl)benzyloxy]-tert-butyldimethylsilane 

Downstream Products

• 844868-79-7 7-{2-[4-(8-hydroxy-3,7-dimethylocta-6,7-dienyl)-3,5-bis(methoxymethoxy)phenyl]vinyl}-5-methoxy-1,1,4a-trimethyl-2,3,4,4a,9,9a-hexahydro-1H-xanthen-2-ol 
• 844868-76-4 (6'R)-4-hydroxy-3-methoxy-5-(3',7'-dimethyl-6',7'-epoxy-2'-octenyl)benzyl alcohol 

Relevant academic research and scientific papers

Synthesis of nonracemic 3-deoxyschweinfurthin B

(Chemical Equation Presented) Synthesis of nonracemic 3-deoxyschweinfurthin B has been accomplished through a synthetic sequence including a key cascade cyclization of an epoxy olefin. The intermediate epoxide could be prepared as a single enantiomer thro

SCHWEINFURTHIN ANALOGUES

Methods and intermediates for preparing enantiomerically enriched Schweinfurthin analogs which are useful for the treatment of cancer, as well as novel Schweinfurthin analogs having anti-cancer activity, compositions comprising such analogs and therapeuti