844868-79-7

Upstream product

• 865761-69-9 [4-(8-hydroxy-3,7-dimethylocta-2,6-dienyl)-3,5-bis(methoxymethoxy)benzyl]phosphonic acid diethyl ester 
• 844868-78-6 (7R,8aR,10aR)-7-Hydroxy-4-methoxy-8,8,10a-trimethyl-5,7,8,8a,9,10a-hexahydro-6H-xanthene-2-carbaldehyde 
• 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 
• 844868-75-3 [4-(tert-butyl(dimethyl)silyloxy)-5-methoxy-3-(3',7'-dimethyl-6',7'-epoxy-2'-octenyl)benzyloxy](tert-butyl)(dimethyl)silane 
• 844868-77-5 (2R,4aR,9aR)-7-Hydroxymethyl-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 
• 474970-89-3 [4-(tert-butyldimethylsiloxy)-5-methoxy-3-(3',7'-dimethyl-2',6'-octadienyl)benzyloxy]-tert-butyldimethylsilane 
• 865761-93-9 {4-[8-(tert-butyldiphenylsilanyloxy)-3,7-dimethylocta-2,6-dienyl]-3,5-bis(methoxymethoxy)benzyl}phosphonic acid diethyl ester 
• 865761-92-8 tert-butyl-{8-[4-iodomethyl-2,6-bis(methoxymethoxy)phenyl]-2,6-dimethylocta-2,6-dienyloxy}diphenylsilane 
• 865761-91-7 {4-[8-(tert-butyldiphenylsilanyloxy)-3,7-dimethylocta-2,6-dienyl]-3,5-bis(methoxymethoxy)phenyl}methanol 
• 127969-90-8 (2E,6E)-8-((tert-butyldiphenylsilyl)oxy)-3,7-dimethylocta-2,6-dien-1-ol 
• 881075-33-8 (2E,6E)-8-(tert-butyldiphenylsilyloxy)geranyl bromide 

Relevant academic research and scientific papers

Synthesis and structure-activity studies of schweinfurthin B analogs: Evidence for the importance of a D-ring hydrogen bond donor in expression of differential cytotoxicity

The synthesis and biological evaluation of several enantioenriched schweinfurthin B analogs were undertaken to develop structure-activity relationships and guide design of probes for their putative molecular target. The desired stilbenes contain a common

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