145014-10-4

Upstream product

• 145014-09-1 (Δ^2,3E,Δ^6,7E)-8-bromo-1-O-tert-butyldiphenylsilyl-3,7-dimethyl-octa-2,6-dien-1-ol 
• 5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene 
• 24034-73-9 Geranylgeraniol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 412347-67-2 Methanesulfonic acid (2E,6E)-8-(tert-butyl-diphenyl-silanyloxy)-2,6-dimethyl-octa-2,6-dienyl ester 
• 117638-13-8 (Δ^2,3E,Δ^6,7E)-1-O-tert-butyldiphenylsilyl-3,7-dimethyl-octa-2,6-dien-1,8-diol 

Downstream Products

• 145014-11-5 tert-Butyl-((2E,6E,10E,14E)-3,7,11,15,19-pentamethyl-icosa-2,6,10,14,18-pentaenyloxy)-diphenyl-silane 
• 22488-05-7 geranylfarnesol 
• 1355640-88-8 (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene 
• 1355640-89-9 (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14,15-epoxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene 

Relevant academic research and scientific papers

Biomimetic cyclization of epoxide precursors of indole mono-, sesquiand diterpene alkaloids by lewis acids

Cyclization of the synthesized epoxide precursors of indole mono-, sesqui- and diterpene alkaloids was performed to elucidate the mechanism for biomimetic cationic cyclization to polycyclic structures. 3-(6,7- Epoxygeranyl)indole (11), 3-(10,11-epoxyfarne

A simple synthetic process for the elaboration of oligoprenols by stereospecific coupling of di-, tri-, or oligoisoprenoid units

An effective method of allyl-allyl coupling which is position and stereospecific leads in a simple way to oligoprenols from E-allylic halides.