Nithyanandhan, ayaraj ; Jayaraman, Narayanaswamy (2006) Efficient halogen-lithium exchange reactions to functionalize poly(alkyl aryl ether) dendrimers Tetrahedron, 62 (26). pp. 6228-6235. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2006.04.052
Abstract
Poly(alkyl aryl ether) dendrimers were functionalized with bromophenyl groups at their peripheries, so as to have 3, 6, 12, and 24 groups in the zero, first, second, and third generation dendrimers, respectively. The new bromophenyl functionalized dendrimers were assessed for their reactivities in C-heteroatom and C-C bond forming reactions. For this purpose, the bromophenyl functionalized dendrimers were converted quantitatively to their polylithiated derivatives, using n-BuLi in benzene. The polylithiated dendrimers were reacted either with D2O or with CO2, so as to afford the corresponding deuterated and carboxylic acid functionalized dendrimers, respectively. The carboxylic acid functionalized dendrimers were modified further to the methyl esters during their characterization.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Alkylation; C-C bond formation; Dendrimers; Lithiation |
ID Code: | 65988 |
Deposited On: | 20 Oct 2011 07:12 |
Last Modified: | 20 Oct 2011 07:12 |
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