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- W2078392405 abstract "By taking advantage of the orthogonal nature of thiol−ene coupling and anhydride based esterification reactions, a facile and chemoselective strategy to dendritic macromolecules has been developed. The ability to interchange growth steps based on thiol−ene and anhydride chemistry allows the synthesis of fifth-generation dendrimers in only five steps and under benign reaction conditions. In addition, the presented coupling chemistries eliminate the traditional need for protection/deprotection steps and afford dendrimers in high yield and purity. The modularity of this strategy coupled with the latent reactivity of the alkene/hydroxyl chain ends was demonstrated by using different cores (alkene and hydroxyl functional), various AB2 and CD2 monomers and a range of chain end groups. As a result, three dendritic libraries were prepared which exhibited tunability of both the chemical functionality and physical properties including the fabrication of PEG hydrogels." @default.
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- W2078392405 date "2010-07-01" @default.
- W2078392405 modified "2023-10-12" @default.
- W2078392405 title "Accelerated Growth of Dendrimers via Thiol−Ene and Esterification Reactions" @default.
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- W2078392405 doi "https://doi.org/10.1021/ma1009935" @default.
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