1120367-85-2

Upstream product

• 2227-29-4 chlorodiisopropylsilane 
• 104713-12-4 (R)-1-phenylprop-2-en-1-ol 

Downstream Products

• 1120367-82-9 N-(2-{[(2S,3R,6S)-6-[(diisopropyl((R)-1'-phenylallyloxy)silyloxy)methyl]-2-methoxy-3,6-dihydro-2H-pyran-3-yloxy]methyl}allyl)-N-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-4-methylbenzenesulfonamide 
• 1127305-95-6 (1''R,2''R,3''S,4''S,1'''R)-N-[2-((Z)-4'-{[3''-((diisopropyl-{1'''-phenyl-allyloxy}-silanyloxy)methyl)-7''-oxa-bicyclo[2.2.1]hept-5''-en-2''-ylmethoxy]-diisopropyl-silanyloxy}-but-2'-enyloxymethyl)-allyl]-N-(3'''',3'''',4'''',4'''',5'''',5'''',6'''',6'''',7'''',7'''',8'''',8'''',9'''',9'''',10'''',10'''',10''''-heptadecafluorodecyl)-4'''''-methyl-benzenesulfonamide 
• 1127305-35-4 (Z)-(1'R,4'R,1''R)-N-{4'-[diisopropyl(1''-phenylallyloxy)silyloxy]cyclopent-2'-en-1'-yl}-N-{4-[2-((N'-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-4-methylbenzenesulfonamido)methylallyloxy]but-2-enyl}-2-nitrobenzenesulfonamide 

Relevant academic research and scientific papers

An efficient method for synthesising unsymmetrical silaketals: Substrates for ring-closing, including macrocycle-closing, metathesis

Diisopropylsilyl ethers were activated with N-bromosuccinimide, and reacted with a fluorous-tagged alcohol, to yield tethered substrates for ring-closing metathesis reactions. The Royal Society of Chemistry.