182058-88-4

Upstream product

• 220786-64-1 3,5-bis(allyloxy)benzyl chloride 
• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 177837-80-8 3,5-bis(prop-2-en-1-yloxy)benzyl alcohol 
• 135710-38-2 3,5-bis(2-propen-1-yloxy)benzoic acid methyl ester 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 789490-57-9 3,5-bis[3,5-bis(2-propen-1-yloxy)benzyloxy]benzoic acid methyl ester 

Downstream Products

• 789490-59-1 3,5-bis{3,5-bis[3,5-bis(2-propen-1-yloxy)benzyloxy]benzyloxy}benzoic acid methyl ester 
• 1012786-71-8 3,5-bis[3,5-bis-(allyloxy)benzyloxy]benzyl chloride 

Relevant academic research and scientific papers

Synthesis of Fréchet-type poly(aryl ether) dendrimers with allyl end groups: Comparative convergent and divergent approaches

The high versatility of allyl groups at the dendrimer periphery makes it important to improve the methodologies to obtain them. Fréchet-type poly(aryl ether) first and second generation dendrimers bearing a conjugated phloroglucinol core with 6 or 12 peri

Polyanionic aryl ether metallodendrimers based on cobaltabisdicarbollide derivatives. Photoluminescent properties

Fluorescent Frechet-type poly(aryl ether) dendrimers that incorporate the 1, 3, 5-triphenylbenzene as core molecule and 3, 6, 9, or 12 terminal allyl ether groups have been prepared in very good yield by following the Frechet convergent approach. Regiospe

Cross-linking dendrimers with allyl ether end-groups using the ring-closing metathesis reaction

A third generation Frechet-type dendrimer containing 24 allyl ether end-groups was synthesized, cross-linked using the ring-closing metathesis (RCM) reaction, and the core was removed hydrolytically without significant fragmentation. The results are analo