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Title of Article

SYNTHESIS OF BIOCONJUGATES FOR BORON NEUTRON CAPTURE THERAPY OF CANCER BASED ON COBALT BIS(1,2-DICARBOLLIDE) VIA THE [3+2] CU(I) CATALYZED CYCLOADDITION OF AZIDES TO ALKYNES


Issue
3
Date
2013

Article type
scientific article
UDC
546.271+546.73+547.791
Pages
110-114
Keywords
cobalt bis(1,2-dicarbollide), azides, terminal acetylenes, 1,2,3-triazoles, click chemistry methods, halogenation.


Authors
Kosenko Irina Dmitrievna
Institut elementoorganicheskikh soedineniy im. A.N. Nesmeyanova RAN, Moskva

Lobanova Irina Anatolevna
Institut elementoorganicheskikh soedineniy im. A.N. Nesmeyanova RAN, Moskva

Bregadze Vladimir Iosifovich
Institut elementoorganicheskikh soedineniy im. A.N. Nesmeyanova RAN, Moskva


Abstract
The paper describes the synthesis of 1,2,3-triazole derivatives of bis (1,2-dicarbollide) cobalt using 1,3-dipolar cycloaddition reaction of [3 +2] cycloaddition, namely the «click»-methodology. It is shown that the interaction of azido derivatives of cobalt bis (1,2-dicarbollide) with derivatives of cobalt bis (1,2-dicarbollide) with a terminal acetylene group leads to 1,2,3-triazoles with metal carboran substitutes at sites 1 and 4. The possibility is shown of introducing a halogen into the metal carboran substitute of the synthesized 1,2,3-triazoles.

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