Related Experiment Video
Updated: Mar 30, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
Published on: August 12, 2019
Catalytic addition of amines to carbodiimides by bis(β-diketiminate)lanthanide(II) complexes and mechanistic studies
Mingqiang Xue1, Yu Zheng1, Yubiao Hong1
1Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Dushu Lake Campus, Soochow University, Suzhou 215123, People's Republic of China. xuemingqiang@suda.edu.cn xufan@suda.edu.cn.
Abstract:
Reduction reactions of bis(β-diketiminate)lanthanide(III) chlorides formed in situ by reactions of anhydrous LnCl3 with 2 equiv. of sodium salt of the β-diketiminate ligand in THF with a Na/K alloy afforded a series of bis(β-diketiminate)lanthanide(II) complexes LnL2(THF)n (L = L(2,6-Me2) = [N(2,6-Me2C6H3)C(Me)]2CH(-), n = 1, Ln = Eu (1); L = L(2,4,6-Me3) = [N(2,4,6-Me3C6H2)C(Me)]2CH(-), n = 1, Ln = Eu (2); L = L(2,6-iPr2) = [N(2,6-(i)Pr2C6H3)C(Me)]2CH(-), n = 0, Ln = Eu (3), Sm (4); L = L(2,6-ipr2)(Ph) = [(2,6-(i)Pr2C6H3)NC(Me)CHC(Me)N(C6H5)](-), n = 0, Ln = Eu (5), Yb (6); L = L(2-Me) = [N(2-MeC6H4)C(Me)]2CH(-), n = 1, Ln = Yb (7)) in high yields. All the complexes, especially the complexes of Sm(II) (4) and Eu(II) (5), were found to be excellent pre-catalysts for catalytic addition of amines to carbodiimides to multi-substituted guanidines with a wide scope of substrates. The activity depends both on the central metals and the ligands with the active sequence of Yb(II) < Eu(II) and Eu(II) < Sm(II) and L(2,6-Me2) < L(2,4,6-Me3) ∼ L(2,6-iPr2) < L(2,6-ipr2)(Ph) for the ligands. The mechanistic study by the isolation of guanidinate species and their reactivity revealed that Eu(II) monoguanidinate complexes Eu(L(2,6-Me2))[(C6H5N)C(NHCy)(NCy)](DME) (8) and Eu(L(2,6-ipr2)Ph)[(C6H5N)C(NHCy)(NCy)](THF)2 (9) should be the key active intermediates for the systems with Eu(II) complexes and a Yb(III) bis(guanidinate) complex Yb(L(2-Me))[(C6H5N)C(NHCy)(NCy)]2 (11) for the system using a Yb(II) complex.
More Related Videos
10:17Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
07:06A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
Related Concept Videos
Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview
Aldehydes and Ketones with Amines: Imine Formation Mechanism
Imines are formed under mildly acidic conditions. A pH of 4.5 is ideal for the reaction.
If the pH is low or the solution is too acidic, the reaction slows down in the...
Amides to Amines: LiAlH4 Reduction
Amide reduction requires two equivalents of the reducing agent, acting as a source of hydride ions. As shown in the figure, the reaction is initiated with a nucleophilic attack by the hydride ion at the carbonyl carbon to form a tetrahedral intermediate.
Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)
Conjugate addition results in a thermodynamically stable product. The reaction retains the stronger C=O bond at the expense of the weaker C=C π bond. The process is slow as the β carbon is less electrophilic than the carbonyl carbon.
Direct addition products are...
Conjugate Addition to α,β-Unsaturated Carbonyl Compounds
Preparation of Amines: Reductive Amination of Aldehydes and Ketones