Azido- and ethynyl-substituted 2,2′:6′,2″-terpyridines as suitable substrates for click reactions

Synthesis

Volumn , Issue 9, 2009, Pages 1506-1512

  Winter, Andreas ^a   Wild, Andreas ^b   Hoogenboom, Richard ^a   Fijten, Martin W M ^a   Hager, Martin D ^b   Fallahpour, Reza Ali ^c   Schubert, Ulrich S ^a,b  

^a EINDHOVEN UNIVERSITY OF TECHNOLOGY   (Netherlands)

^b FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^c HetCat   (Switzerland)

Author keywords

Click reaction; Complexes; Cycloaddition; Ligands; Terpyridines

Indexed keywords

BUILDING BLOCK; CLICK REACTION; COMPLEXES; END-GROUP MODIFICATION; ETHYNYL; FUNCTIONALIZED; FUNCTIONALIZED POLYMERS; MACRO LIGAND; SUPRAMOLECULAR ASSEMBLIES; TERPYRIDINE; TERPYRIDINES;

BUILDING MATERIALS; FUNCTIONAL MATERIALS; LIGANDS; NITROGEN COMPOUNDS;

FUNCTIONAL POLYMERS;

4 [1 (2,2':6',2'' TERPYRIDIN 4' YL) 1H 1,2,3 TRIAZOL 4 YL]BENZALDEHYDE; 4 [4 POLY(2 ETHYLOXAZOLINE) 1H 1,2,3 TRIAZOL 1 YL] 2,2':6',2'' TERPYRIDINE; 4' (4 PHENYL 1H 1,2,3 TRIAZOL 1 YL) 2,2':6',2'' TERPYRIDINE; 4' [4 [1 (10 BROMOANTHRACEN 9 YL) 1H 1,2,3 TRIAZOL 4 YL]PHENYL] 2,2':6',2'' TERPYRIDINE; 4' [4 [1 (2,2':6',2'' TERPYRIDIN 4' YL) 1H 1,2,3 TRIAZOL 4 YL]PHENYL] 2,2':6',2'' TERPYRIDINE; 4' [4 [1 (4 BROMOPHENYL) 1H 1,2,3 TRIAZOL 4 YL]PHENYL] 2,2':6',2'' TERPYRIDINE; 4' AZIDO 2,2':6',2'' TERPYRIDINE; [1 (2,2':6',2'' TERPYRIDIN 4' YL) 1H 1,2,3 TRIAZOL 4 YL]METHANOL; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; GEL PERMEATION CHROMATOGRAPHY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; SUBSTITUTION REACTION; SYNTHESIS;

EID: 67650045472     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1088159     Document Type: Article

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