Journal
ORGANOMETALLICS
Volume 31, Issue 7, Pages 2764-2769Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om201060e
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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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