Effect of Benzylic Methyl Groups on Kinetic Basicity of Amine Ligand ino-Boron SubstitutedN,N-Dimethylbenzylamines
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/72/8/72_8_1879/_pdf
Reference33 articles.
1. 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
2. Dynamic NMR as a Nondestructive Method for the Determination of Rates of Dissociation. XX. Secondary Isotope Effect on Kinetic Basicity of Amine Ligands in Boronate–Amine Complexes and Ammonium Salts
3. Experimental and Theoretical Evidence of an SN2-Type Mechanism for Dissociation of B−N Coordination Bonds in 2,6-Bis((dimethylamino)methyl)phenylborane Derivatives1
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. Steric consequence of the diastereoselective addition of chiral lithium 2-(1-dimethylaminoethyl)phenyl cuprates to some enones
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