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Org Lett ; 9(19): 3713-6, 2007 Sep 13.
Article in English | MEDLINE | ID: mdl-17696438

ABSTRACT

We report the application of "click" chemistry for the synthesis of hybrid calixarenes appended on the upper rim with carbohydrate and N,C-protected alpha-amino acids. The chemoselective N- or C-deprotection of the alpha-amino acids and their subsequent transformation into dipeptides is described. The first example of a chemo-enzymatic synthesis on upper rim derived calix[4]arenes using trans-sialidase affords sialylated lactose calix[4]arenes. Our innovative chemo-enzymatic process paves the way for further applications.


Subject(s)
Calixarenes/chemistry , Calixarenes/chemical synthesis , Animals , Calixarenes/metabolism , Carbohydrates/chemistry , Glycoproteins/metabolism , Microwaves , Molecular Structure , Neuraminidase/metabolism , Trypanosoma cruzi/enzymology
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