Transition-metal-carbene-like intermolecular insertion of a borylene into C–H bonds†
Abstract
We demonstrate that, in analogy to transition-metal carbene chemistry, [(OC)5Mo![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) BN(SiMe3)2] facilitates intermolecular transfer of the borylene [:BN(SiMe3)2], which ultimately undergoes insertion into C–H bonds under very mild conditions. The one-pot multiple functionalization of the cyclopentadienyl rings of tungstenocene dihydride is demonstrated using this approach.
BN(SiMe3)2] facilitates intermolecular transfer of the borylene [:BN(SiMe3)2], which ultimately undergoes insertion into C–H bonds under very mild conditions. The one-pot multiple functionalization of the cyclopentadienyl rings of tungstenocene dihydride is demonstrated using this approach.
- This article is part of the themed collections: Celebrating our 2021 Prizewinners and Editor’s Choice: Main group reagents and catalysts in organic reactions
 
                




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