A number of 3-alkyl-substituted 1,2-dicarba- closo -dodecaboranes were prepared in good yields via the reaction of alkyldichloroboranes, which were generated in situ through hydroboration of the corresponding alkenes with a dichloroborane–dioxane complex, with thallium dicarbollides in anhydrous dichloromethane at room temperature. This reaction also affords insertion products with new thallium dicarbollides prepared from 3-iodo- and 9-iodo-1,2-dicarba- closo -dodecaboranes. The synthesized 3-alkyl-1,2-dicarba- closo -dodecaboranes can be selectively deboronated at the B(6) atom to form the anionic 3-alkyl-7,8-dicarba- nido -undecaborates. All compounds were characterized by NMR and MS techniques.
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Safronov et al. (2012) studied this question.
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