The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles)

Weber L (2001)
Coordination Chemistry Reviews 215(1): 39-77.

Journal Article | Published | English

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Abstract
1,3,2-Diazaborolines (2,3-dihydro-1H-1,3,2-diazaboroles) are at the interface between inorganic, organometallic and organic chemistry. The planar rings with 6 pi -electrons may be regarded as heteroarenes, as evidenced by NMR and photoelectron spectra and confirmed by quantum mechanical calculations. The capability of 1,3,2-diazaborolines to act as eta (5)-ligands adds chemical proof to this idea. High-yield syntheses of 1,3,2-diazaborolines with functional groups at boron have recently become available, providing a rich area of chemistry ranging from substitution processes via borylstannations to their conversion into oxazaborolidines. (C) 2001 Elsevier Science B.V. All rights reserved.
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Weber L. The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles). Coordination Chemistry Reviews. 2001;215(1):39-77.
Weber, L. (2001). The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles). Coordination Chemistry Reviews, 215(1), 39-77.
Weber, L. (2001). The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles). Coordination Chemistry Reviews 215, 39-77.
Weber, L., 2001. The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles). Coordination Chemistry Reviews, 215(1), p 39-77.
L. Weber, “The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles)”, Coordination Chemistry Reviews, vol. 215, 2001, pp. 39-77.
Weber, L.: The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles). Coordination Chemistry Reviews. 215, 39-77 (2001).
Weber, Lothar. “The chemistry of 1,3,2-diazaborolines (2,3-dihydro-1H-l,3,2-diazaboroles)”. Coordination Chemistry Reviews 215.1 (2001): 39-77.
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