| Literature DB >> 30276985 |
Tom E Stennett1,2, Rüdiger Bertermann1,2, Holger Braunschweig1,2.
Abstract
Sterically unencumbered diborenes based on a benzylphosphine chelate undergo diboration reactions with bis(catecholato)diboron in the absence of a catalyst to yield tetraboranes. The symmetrical diborenes studied undergo 1,2-diborations, whereas an unsymmetrical derivative was found to yield a triborylborane-phosphine adduct as the result of a formal 1,1-diboration. A related borylborylene compound also underwent a 1,2-diboration to produce a borylene-borane adduct.Entities:
Keywords: boron; chain structures; diboration; isomers; low-valent compounds
Year: 2018 PMID: 30276985 DOI: 10.1002/anie.201809976
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336