Abstract
2,3-Bis(dimethylamino)-substituted B2N2C2heterocycles underwent selective dimethylamino/hydride exchange with either one or two equivalents of BH3⋅SMe2to give the corresponding cyclic monohydrido- or (cis)1,2-dihydridodiboranes(4), respectively. Upon either heating or irradiation in solution, the latter underwent ring contraction to the corresponding five-membered BN2C2heterocycles, whereas irradiation of the 1,2-dimethylaminoethene-supported 1,2-dihydridodiborane(4) in the presence of PEt3gave an unprecedented unsymmetrical 1,1-dihydrodiborane(5) phosphine adduct.
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Arrowsmith, M., Braunschweig, H., Radacki, K., Thiess, T., & Turkin, A. (2017). Facile Access to Unprecedented Electron-Precise Monohydrodiboranes(4), cis-1,2-Dihydrodiboranes(4), and a 1,1-Dihydrodiborane(5). Chemistry - A European Journal, 23(9), 2179–2184. https://doi.org/10.1002/chem.201605270
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