New Approach to the Synthesis of 3-Alkyl-1,2-dicarba-closo-dodecaboranes: Reaction of Alkyldichloroboranes with Thallium Dicarbollide
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 dichl...
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Veröffentlicht in: | Organometallics 2012-04, Vol.31 (7), p.2764-2769 |
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creator | Safronov, Alexander V Shlyakhtina, Natalia I Hawthorne, M. Frederick |
description | 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. |
doi_str_mv | 10.1021/om201060e |
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Frederick</creator><creatorcontrib>Safronov, Alexander V ; Shlyakhtina, Natalia I ; Hawthorne, M. Frederick</creatorcontrib><description>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. 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Frederick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Approach to the Synthesis of 3-Alkyl-1,2-dicarba-closo-dodecaboranes: Reaction of Alkyldichloroboranes with Thallium Dicarbollide</atitle><jtitle>Organometallics</jtitle><addtitle>Organometallics</addtitle><date>2012-04-09</date><risdate>2012</risdate><volume>31</volume><issue>7</issue><spage>2764</spage><epage>2769</epage><pages>2764-2769</pages><issn>0276-7333</issn><eissn>1520-6041</eissn><abstract>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.</abstract><pub>American Chemical Society</pub><doi>10.1021/om201060e</doi><tpages>6</tpages></addata></record> |
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title | New Approach to the Synthesis of 3-Alkyl-1,2-dicarba-closo-dodecaboranes: Reaction of Alkyldichloroboranes with Thallium Dicarbollide |
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