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.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
Abstract / Bemerkung
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.
Erscheinungsjahr
Zeitschriftentitel
Coordination Chemistry Reviews
Band
215
Zeitschriftennummer
1
Seite
39-77
ISSN
PUB-ID

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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. doi:10.1016/S0010-8545(00)00402-1
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.