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Issue 12, 2013
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Synthesis of new ω-amino- and ω-azidoalkyl carboranes

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Abstract

Novel carboranyl amines [7-NH2(CH2)nS-7,8-C2B9H11] were synthesized by alkylation of 1-mercapto-ortho-carborane with ω-bromoalkylphthalimides followed by removal of the protecting group with hydrazine. closo-Carboranyl azides 1-N3(CH2)nS-1,2-C2B10H11 were prepared by the reaction of the corresponding carboranyl alcohol/iodide with sodium azide and converted to the water soluble nido-form [7-N3(CH2)nS-7,8-C2B9H11] with ammonium formate in refluxing methanol.

Graphical abstract: Synthesis of new ω-amino- and ω-azidoalkyl carboranes

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Publication details

The article was received on 22 Jun 2013, accepted on 02 Oct 2013 and first published on 03 Oct 2013


Article type: Letter
DOI: 10.1039/C3NJ00677H
Citation: New J. Chem., 2013,37, 3865-3868
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    Synthesis of new ω-amino- and ω-azidoalkyl carboranes

    M. Yu. Stogniy, I. B. Sivaev, I. A. Godovikov, Z. A. Starikova, V. I. Bregadze and S. Qi, New J. Chem., 2013, 37, 3865
    DOI: 10.1039/C3NJ00677H

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