CAN catalysis and click chemistry routes in the synthesis of carborane-containing ferrocenes

被引:4
作者
Ol'shevskaya, Valentina A. [1 ]
Makarenkov, Anton V. [1 ]
Borisov, Yury A. [1 ]
Ananyev, Ivan V. [1 ]
Kononova, Elena G. [1 ]
Kalinin, Valery N. [1 ]
Ponomaryov, Andrey B. [1 ]
机构
[1] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, 28 Vavilova Str, Moscow 119991, Russia
基金
俄罗斯基础研究基金会;
关键词
Ferrocene; Carborane; CAN catalysis; Triazoles; DFT calculation; MEDICINAL CHEMISTRY; BIOORGANOMETALLIC CHEMISTRY; 1,3-DIPOLAR CYCLOADDITION; ANTIMALARIAL ACTIVITY; ELECTRONIC-PROPERTIES; BORON CLUSTERS; DRUG DISCOVERY; DESIGN; DERIVATIVES; PHARMACOPHORES;
D O I
10.1016/j.poly.2017.11.034
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
CAN-catalyzed reactions between alpha-ferrocenyl ethanol or ferrocenyl methanol and S-, N- and O-carborane nucleophiles are reported. This approach is an efficient and simple procedure for the preparation of carborane derivatives containing ferrocenyl units. Energy and geometry optimizations of some carboranylthio-, carboranylamino- and carboranyloxy-substituted ferrocenes have been calculated using the density functional theory. A series of new ferrocene-containing carborane 1,2,3-triazoles have been synthesized in good yields through a facile copper-mediated 1,3-dipolar cycloaddition reactions of alkynyl ferrocenes with [(o-carboran-1-yl)methyl]azide. Molecular structure of carborane-substituted ferrocenyl triazole was established by single crystal X-ray diffraction study. Representative examples of all ferrocenyl carboranes prepared were characterized by IR, H-1 and B-11 NMR spectroscopy. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:181 / 190
页数:10
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