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Issue 47, 2015
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sp2–sp3 diboranes: astounding structural variability and mild sources of nucleophilic boron for organic synthesis

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Abstract

Despite the widespread use of organoborane reagents in organic synthesis and catalysis, a major challenge still remains: very few boron-centered nucleophiles exist for the direct construction of B–C bonds. Perhaps the most promising emerging solution to this problem is the use of sp2–sp3 diboranes, in which one boron atom of a conventional diborane(4) is quaternised by either a neutral or anionic nucleophile. These compounds, either isolated or generated in situ, serve as relatively mild and convenient sources of the boryl anion [BR2] for use in organic synthesis and have already proven their efficacy in metal-free as well as metal-catalysed borylation reactions. This Feature article documents the history of sp2–sp3 diborane synthesis, their properties and surprising structural variability, and their burgeoning utility in organic synthesis.

Graphical abstract: sp2–sp3 diboranes: astounding structural variability and mild sources of nucleophilic boron for organic synthesis

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Publication details

The article was received on 19 Mar 2015, accepted on 17 Apr 2015 and first published on 20 Apr 2015


Article type: Feature Article
DOI: 10.1039/C5CC02316E
Citation: Chem. Commun., 2015,51, 9594-9607

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    sp2–sp3 diboranes: astounding structural variability and mild sources of nucleophilic boron for organic synthesis

    R. D. Dewhurst, E. C. Neeve, H. Braunschweig and T. B. Marder, Chem. Commun., 2015, 51, 9594
    DOI: 10.1039/C5CC02316E

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