246512-25-4

Upstream product

• 137472-14-1 methyl 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy] benzoate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 80457-61-0 methanesulfonyl 3,5-dibenzyloxybenzyl alcohol 
• 24131-32-6 3,5-bis(benzyloxy)benzyl bromide 
• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 129536-40-9 [3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-methanol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 137472-16-3 [3,5-bis[[3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]phenyl]methoxy]phenyl]methyl alcohol 
• 779332-28-4 4'-[3,5-bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-[2,2';6',2'']terpyridine 
• 129536-41-0 3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyl bromide 
• 278610-81-4 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol 

Relevant academic research and scientific papers

Dendrimer analogues of linear molecules to evaluate energy and charge-transfer properties

We have designed and synthesized difunctionalized dendrimers containing two donors in the periphery and an acceptor at the core to serve as scaffolds for comparison with linear analogues to investigate the advantage of dendritic scaffolds for energy and c

Alternative convergent and accelerated double-stage convergent approaches towards functionalized dendritic polyethers

Alternative convergent synthesis strategies for the preparation of dendritic macromolecules, using either mesylate activation or the Mitsunobu reaction, are described. The synthesis can be further accelerated by using a double stage convergent approach. T