One-pot procedure for diazo transfer and azide-alkyne cycloaddition: Triazole linkages from amines

被引:142
作者
Beckmann, Henning S. G. [1 ]
Wittmann, Valentin [1 ]
机构
[1] Univ Konstanz, Fachbereich Chem, D-78457 Constance, Germany
关键词
D O I
10.1021/ol0621506
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A one-pot reaction for Cu(II)-catalyzed diazo transfer and Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition (sometimes called click reaction) is reported. 1,4-Disubstituted 1,2,3-triazoles are obtained in excellent yields from a variety of readily available amines without the need for isolation of the azide intermediates. The reaction has a broad scope and is especially practical for the synthesis of multivalent structures because compounds substituted with multiple azides are potentially unstable.
引用
收藏
页码:1 / 4
页数:4
相关论文
共 47 条
[41]   Bioconjugation by copper(I)-catalyzed azide-alkyne [3+2] cycloaddition [J].
Wang, Q ;
Chan, TR ;
Hilgraf, R ;
Fokin, VV ;
Sharpless, KB ;
Finn, MG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (11) :3192-3193
[42]   Copper-catalyzed reaction cascade:: Direct conversion of alkynes into N-sulfonylazetidin-2-imines [J].
Whiting, Matthew ;
Fokin, Valery V. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (19) :3157-3161
[43]   Spatial screening of cyclic neoglycopeptides: Identification of polyvalent wheat-germ agglutinin ligands [J].
Wittmann, V ;
Seeberger, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (07) :900-903
[44]  
Wittmann V, 2000, ANGEW CHEM INT EDIT, V39, P4348, DOI 10.1002/1521-3773(20001201)39:23<4348::AID-ANIE4348>3.0.CO
[45]  
2-X
[46]  
Wittmann V., 2004, Highlights in Bioorganic Chemistry: Methods and Applications, P203, DOI DOI 10.1002/3527603727.CH2G
[47]   Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(I)-catalyzed ligation of azides and alkynes [J].
Wu, P ;
Feldman, AK ;
Nugent, AK ;
Hawker, CJ ;
Scheel, A ;
Voit, B ;
Pyun, J ;
Fréchet, JMJ ;
Sharpless, KB ;
Fokin, VV .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (30) :3928-3932