期刊
COORDINATION CHEMISTRY REVIEWS
卷 215, 期 -, 页码 39-77出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/S0010-8545(00)00402-1
关键词
heterocycles; diazaborolines; cyclocondensation; dehydrogenation; displacement reactions; borylstannation
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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