Synthesis of Symmetrical and Unsymmetrical PAMAM Dendrimers by Fusion between Azide- and Alkyne-Functionalized PAMAM Dendrons
- 1 March 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Bioconjugate Chemistry
- Vol. 18 (2) , 579-584
- https://doi.org/10.1021/bc060256f
Abstract
A new convergent synthetic method for the synthesis of PAMAM dendrimers has been developed. The fusion between propargyl-functionalized PAMAM dendrons and azido-functionalized PAMAM dendrons via the Cu(I)-catalyzed Huisgen [2 + 3] dipolar cycloaddition reaction (click chemistry) of an alkyne and an azide leads to the formation of symmetric PAMAM dendrimers in high yields. Furthermore, the coupling reactions between the different generation dendrons afford the size-differentiated unsymmetrical PAMAM dendrimers.Keywords
This publication has 6 references indexed in Scilit:
- Convergent Synthesis of Internally Branched PAMAM DendrimersOrganic Letters, 2005
- Nanomedicine: current status and future prospectsThe FASEB Journal, 2004
- Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to AzidesThe Journal of Organic Chemistry, 2002
- Convergent Dendrons and Dendrimers: from Synthesis to ApplicationsChemical Reviews, 2001
- Preparation of polymers with controlled molecular architecture. A new convergent approach to dendritic macromoleculesJournal of the American Chemical Society, 1990
- A New Class of Polymers: Starburst-Dendritic MacromoleculesPolymer Journal, 1985