881075-33-8

Upstream product

• 127969-90-8 (2E,6E)-8-((tert-butyldiphenylsilyl)oxy)-3,7-dimethylocta-2,6-dien-1-ol 

Downstream Products

• 947588-46-7 ((2E,6E)-9-(3-bromophenyl)-2,6-dimethyl-9-(phenylsulfonyl)nona-2,6-dienyloxy)(tert-butyl)diphenylsilane 
• 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 
• 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 
• 865761-69-9 [4-(8-hydroxy-3,7-dimethylocta-2,6-dienyl)-3,5-bis(methoxymethoxy)benzyl]phosphonic acid diethyl ester 
• 865761-91-7 {4-[8-(tert-butyldiphenylsilanyloxy)-3,7-dimethylocta-2,6-dienyl]-3,5-bis(methoxymethoxy)phenyl}methanol 

Relevant academic research and scientific papers

CYCLISATION PROCESS OF FORMING A MULTIPLE RING COMPOUND

The present invention relates to a cyclisation process of forming a multiple ring compound from an isoprenoid compound. The cyclisation process involves reacting the isoprenoid compound with an acetal initiator under conditions sufficient to form the multiple ring compound. The isoprenoid compound is contacted with an initiator an optionally with a catalyst. Cyclisation occurs by reaction of the initiator with the isoprenoid compound. Cyclic aceta compounds wherein the acetal forms part of 6-membered unsaturated ring are also defined.

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