506417-46-5

Upstream product

• 100-39-0 benzyl bromide 
• 303014-95-1 7-(tert-butyl-dimethyl-silanyloxy)-hept-1-en-4-ol 
• 87184-81-4 4-(tert-butyldimethylsilanyloxy)butanal 
• 506417-45-4 ethyl 4-(t-butyldimethylsiloxy)butanoate 

Downstream Products

• 506417-56-7 1-((E)-5-Benzyloxy-octa-1,7-dienyl)-4-trifluoromethyl-benzene 
• 506417-50-1 C₂₁H₂₄O₃S 
• 506417-53-4 1-((E)-5-Benzyloxy-octa-1,7-dienyl)-4-nitro-benzene 
• 506417-54-5 1-((E)-5-Benzyloxy-octa-1,7-dienyl)-4-methoxy-benzene 
• 506417-55-6 C₂₁H₂₄O 
• 506417-49-8 (E)-6-Benzyloxy-nona-2,8-dienoic acid ethyl ester 
• 506417-51-2 (E)-7-Benzyloxy-deca-3,9-dien-2-one 
• 506417-52-3 ((Z)-1-Allyl-hex-4-enyloxymethyl)-benzene 
• 506417-48-7 4-benzyloxy-hept-6-enal 
• 478623-08-4 4-(benzyloxy)octa-1,7-diene 
• 506417-47-6 4-(benzyloxy)-6-hepten-1-ol 

Relevant academic research and scientific papers

Relative rate profile for ring-closing metathesis of a series of 1-substituted 1,7-octadienes as promoted by a 4,5-dihydroimidazol-2-ylidene-coordinated ruthenium catalyst

(Matrix presented) This report details the kinetic responses of nine compounds of type 6 to ring-closing metathesis as promoted by 2 to give the identical product 7. The experimental observations have been subjected to Hammett analysis. The ρ value for the composite aromatic derivatives (R = p-XC6H4-) differs from that of the aliphatic series, although both are negative because electron-donating groups accelerate the reaction.