852511-56-9

Upstream product

• 852511-55-8 (Acet)4-[G-2]-OH 
• 768387-51-5 methyl 3,5-bis(prop-2-ynyloxy)benzoate 
• 176038-84-9 3,5-dipropargyloxybenzyl alcohol 
• 176038-86-1 1-(bromomethyl)-3,5-bis(prop-2-ynyloxy)benzene 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 1123207-37-3 methyl 3,5-bis{[3,5-bis(2-propynyloxy)benzyl]oxy}benzoate 

Downstream Products

• 852511-60-5 (Acet)12-([G-2])3-[C] 
• 852511-57-0 (Acet)8-[G-3]-OH 
• 1123207-40-8 methyl 3,5-bis[(3,5-bis{[3,5-bis(2-propynyloxy)benzyl]oxy}benzyl)oxy]benzoate 
• 1395411-43-4 2-(3,5-bis(3,5-bis(prop-2-ynyloxy)benzyloxy)benzyl)isoindoline-1,3-dione 
• 852511-58-1 Acet₈-G₃-Br 

Relevant academic research and scientific papers

Effects of dendron generation and salt concentration on phase structures of dendritic-linear block copolymers with a semirigid dendron containing PEG tails

We prepared a series of dendritic-linear block copolymers (DLBCPs) bearing a semirigid Percec-type dendron with ionophilic poly(ethylene glycol) (PEG) tails and a polystyrene (PS) linear polymer by nitroxide-mediated living radical polymerization (NMRP).

METHOD OF USING CLICK CHEMISTRY TO FUNCTIONALIZE DENDRIMERS

A library of functionalized dendritic macromolecules was prepared in extremely high yields using no protecting group strategies and with only minimal purification steps through the use of copper(l)-catalyzed 1 ,3-dipolar cycloaddition of azides and termin

Structurally diverse dendritic libraries: A highly efficient functionalization approach using click chemistry

The high fidelity and efficiency of Click chemistry are exploited in the synthesis of a library of chain end functionalized dendritic macromolecules. In this example, the selectivity of the Cu-catalyzed [3 + 2π] cycloaddition reaction of azides with termi