224191-95-1

Upstream product

• 224191-80-4 4-triallylmethylphenol 
• 224191-94-0 propionic acid 4-[4-iodo-1,1-bis-(3-iodo-propyl)-butyl]-phenyl ester 
• 224191-89-3 1-(4-allylhepta-1,6-dien-4-yl)-4-methoxybenzene 
• 224191-92-8 p-[1,1-di(3-hydroxypropyl)-4-hydroxybutyl]methoxybenzene 
• 224191-93-9 p-[1,1-di(3-iodopropyl)-4-iodobutyl]phenol 

Downstream Products

• 411240-55-6 C₆₉H₈₉ClO₄ 
• 1144500-85-5 (C₅H₃NCH₂OC₆H₄C((CH₂)3OC₆H₄C(CH₂CHCH₂)3)3)2 
• 411240-61-4 (4-{5-[4-(4-[4-(1,1-diallyl-but-3-enyl)-phenoxy]-1,1-bis-{3-[4-(1,1-diallyl-but-3-enyl)-phenoxy]-propyl}-butyl)-phenoxy]-pentyloxy}-phenyl)-methanol 
• 411240-60-3 C₆₉H₈₉IO₄ 
• 880080-46-6 4-(4-[4-(1,1-dipropyl-butyl)-phenoxy]-1,1-bis-{3-[4-(1,1-dipropyl-butyl)-phenoxy]-propyl}-butyl)-phenol 

Relevant academic research and scientific papers

{FeCp}+-induced hexafunctionalization of hexamethylbenzene with dendrons for the direct synthesis of redox-active iron-centered metallodendrimers

Phenol tri- and nonaallyl dendrons (3 and 7, respectively) were functionalized at the focal position to give the new triallyl dendrons 4 and 6 and the nonaallyl dendrons 11 and 13 that contain a iodoalkyl or a bromobenzyl termini. All these dendrons were

Activation of aryl ethers and aryl sulfides by the Fe(η5-C5H5)+ group for the synthesis of phenol dendrons and arene-centered poly-olefin dendrimers

Organo-iron mediated syntheses of dendrons and dendrimers are described. The reaction of [FeCp(η6-p-EtOC6H4Me)][PF6], 1, with Bu(t)OK or KOH and allyl bromide in THF gives both the triallylation of the acidic Me