z-logo
Premium
Cover Picture: Efficiency and Fidelity in a Click‐Chemistry Route to Triazole Dendrimers by the Copper( I )‐Catalyzed Ligation of Azides and Alkynes (Angew. Chem. Int. Ed. 30/2004)
Author(s) -
Wu Peng,
Feldman Alina K.,
Nugent Anne K.,
Hawker Craig J.,
Scheel Arnulf,
Voit Brigitte,
Pyun Jeffrey,
Fréchet Jean M. J.,
Sharpless K. Barry,
Fokin Valery V.
Publication year - 2004
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200490100
Subject(s) - dendrimer , click chemistry , chemistry , combinatorial chemistry , copper , catalysis , triazole , int , polymer chemistry , organic chemistry , computer science , operating system
Structural diversity is possible in dendrimer syntheses based on the highly efficient construction of triazoles from functionalized azides and alkynes. In their Communication on page 3928 ff., V. V. Fokin et al. describe the application of this Cu I ‐catalyzed transformation, which proceeds in near‐quantitative yields even to the third and fourth generation.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here