Substituent Effects on Configurational Stabilities at Tetrahedral Boron Atoms in Intramolecular Borane–Amine Complexes: Structures, Enantiomeric Resolution, and Rates of Enantiomerization of [2-(Dimethylaminomethyl)phenyl]phenylboranes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference34 articles.
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2. Recent studies on organometallic intramolecular-coordination compounds
3. Dynamic NMR as a Nondestructive Method for the Determination of Rates of Dissociation. XVII. Dissociation of the N–B Bond in the Coordinated Form of 2-[2-(Dimethylaminomethyl)phenyl]-4,4-diphenyl-1,3,2-dioxaborolane and Related Compounds
4. Dynamic NMR as a Nondestructive Method for the Determination of Rates of Dissociation. XVIII. Factors Affecting the Rates of Dissociation of N–B Bond in the Coordinated Form of 9-[2-(Dialkylaminomethyl) phenyl]-9-borabicyclo[3.3.1] nonanes
5. Experimental and Theoretical Evidence of an SN2-Type Mechanism for Dissociation of B−N Coordination Bonds in 2,6-Bis((dimethylamino)methyl)phenylborane Derivatives1
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