The copper-catalyzed alkyne-azide cycloaddition for the construction of fullerene-porphyrin conjugates

被引：4

作者：

Hahn, Uwe

Nierengarten, Jean-Francois ^{[1
]}

机构：

[1] Univ Strasbourg, Lab Chim Mat Mol, 25 Rue Becquerel, F-67087 Strasbourg 2, France

来源：

JOURNAL OF PORPHYRINS AND PHTHALOCYANINES | 2016年 / 20卷 / 8-11期

关键词：

porphyrin; fullerene; azide; alkyne; cycloaddition; click chemistry; DIRECTED REMOTE FUNCTIONALIZATION; ELECTRON-TRANSFER PROCESSES; CLICK CHEMISTRY; STEREOSELECTIVE-SYNTHESIS; LIQUID-CRYSTALLINE; BUILDING-BLOCK; TRIS-ADDUCTS; ORTHOGONAL FUNCTIONALIZATION; REGIOSELECTIVE SYNTHESIS; ENANTIOMERICALLY PURE;

D O I：

10.1142/S1088424616500966

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Click chemistry has become a very popular and efficient concept for synthetic chemists for the construction of new molecules. Among the click chemistry approaches known to date, it is undoubted that the copper-catalyzed alkyne-azide 1,3-dipolar cycloaddition (CuAAC) has played a key role. Such reactions in general offer virtually unlimited possibilities to prepare new molecules for e.g. materials science applications. As such, the synthesis of porphyrin-fullerene conjugates obtained via CuAAC are summarized within the present review article.

引用

页码：918 / 934

页数：17

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