474970-91-7

Upstream product

• 474970-89-3 [4-(tert-butyldimethylsiloxy)-5-methoxy-3-(3',7'-dimethyl-2',6'-octadienyl)benzyloxy]-tert-butyldimethylsilane 
• 2316-61-2 5-bromo-4-hydroxy-3-methoxybenzyl alcohol 
• 474970-83-7 (5-bromo-4-hydroxy-3-methoxybenzyloxy)-tert-butyldimethylsilane 
• 474970-82-6 (5-bromo-4-(tert-butyldimethylsiloxy)-3-methoxybenzyloxy)-tert-butyldimethylsilane 
• 474970-87-1 [4-hydroxy-5-methoxy-3-(3',7'-dimethyl-2',6'-octadienyl)benzyloxy]-tert-butyldimethylsilane 

Downstream Products

• 474970-81-5 4-hydroxy-3-methoxy-5-(3',7'-dimethyl-7'-hydroxy-6'-phenylselenyl-2'-octenyl)benzyl alcohol 
• 474970-93-9 [4-(tert-butyldimethylsiloxy)-5-methoxy-3-(3',7'-dimethyl-7'-hydroxy-6'-phenylselenyl-2'-octenyl)benzyloxy]-tert-butyldimethylsilane 

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

A cascade cyclization approach to schweinfurthin B

(graph presented) A strategy for synthesis of the hexahydroxanthene moiety of the natural products schweinfurthin A, B, and D is described. The relative stereochemistry in the key cationic cyclization step is established through the preference of the phen