- Ytterbium triflate: A highly active catalyst for addition of amines to carbodiimides to N,N′,N″-trisubstituted guanidines
-
(Chemical Equation Presented) Ytterbium triflate was found to be efficient catalyst for addition of amines to carbodiimides to N,N′,N″- trisubstituted guanidines with a wide scope of amines under solvent-free condition.
- Zhu, Xuehua,Du, Zhu,Xu, Fan,Shen, Qi
-
-
Read Online
- Synthesis and Reactivity of NNNNN-Pincer Multidentate Pyrrolyl Rare-Earth-Metal Amido-Chloride or Dialkyl Complexes
-
The NNNNN-pincer multidentate pyrrolyl rare-earth-metal amido-chloride complexes {η1:κ3-2,5-[CH3N(CH2CH2)2NCH2]2C4H2N}RECl[N(SiMe3)2] (RE = Y (2a), Sm (2b), Dy (2c), Er (2d), Yb (2e)) were synthesized by one step from reactions of [(Me3Si)2N]3RE(μ-Cl)Li(T
- Cui, Peng,Du, Jun,Huang, Zeming,Sheng, Weiming,Wang, Shaowu,Wei, Yun,Xu, Xiaolong,Zhang, Lijun,Zhang, Xiuli,Zhou, Shuangliu,Zhu, Xiancui
-
supporting information
p. 4525 - 4534
(2020/12/22)
-
- Cyclic (Alkyl)amino Carbene Complex of Aluminum(III) in Catalytic Guanylation Reaction of Carbodiimides
-
Herein we report the synthesis of a cyclic (alkyl)amino carbene (cAAC) complex of AlMe3. This complex was used as an efficient catalyst for the guanylation reaction of carbodiimides with primary arylamines and secondary amines to deliver guanidine derivatives in good to excellent yields. This catalytic protocol can tolerate a wide range of functional groups. Furthermore, the longevity of the catalyst was tested in successive catalytic cycles, which indicated a sustained catalytic activity over a multiple cycles. The mechanistic pathway was well understood with the help of stoichiometric reaction and DFT study.
- Vardhanapu, Pavan K.,Bheemireddy, Varun,Bhunia, Mrinal,Vijaykumar, Gonela,Mandal, Swadhin K.
-
p. 2602 - 2608
(2018/08/21)
-
- Catalytic C-N bond formation in guanylation reaction by N-heterocyclic carbene supported magnesium(II) and zinc(II) amide complexes
-
The catalytic activity of N-heterocyclic carbene (NHC) supported magnesium(II) and a zinc(II) amide complex towards the addition of N-H bond of amine to carbodiimide was studied. Treatment of a free carbene i.e., 1,3-di-tert-butylimidazol-2-ylidene (ItBu) with magnesium and zinc bis(amide) i.e., M[N(SiMe3)2]2, M = Mg or Zn in toluene led to the formation of ItBu:M[N(SiMe3) 2]2, M = Mg(1) and Zn(2) compounds, respectively. Both 1 and 2 were characterized by multinuclear (1H, 13C and 29Si) NMR spectroscopy and single X-ray crystal structure analysis. Solid state structures revealed that both complexes are monomeric in nature and their magnesium and zinc atoms are three coordinated and distorted trigonal planar in geometries. Furthermore, compounds 1 and 2 were tested as catalysts for the guanylation reaction of addition of amine to carbodiimide and turned to be excellent catalysts.
- Baishya, Ashim,Barman, Milan Kr.,Peddarao, Thota,Nembenna, Sharanappa
-
p. 112 - 118
(2014/09/17)
-
- Enol-functionalized N-heterocyclic carbene lanthanide amide complexes: Synthesis, molecular structures and catalytic activity for addition of amines to carbodiimides
-
Reaction of LnCl3 (Ln = Y, Nd, Sm and Yb) with enol-functionalized imidazolium salt H2LBr (L = 4-OMe-C 6H4COCH{C(NCHCHNiPr)}) and NaN(TMS)2 at a molar ratio of 1:4:1 in THF at room temperature afforded the corresponding novel enol-functionalized N-heterocyclic carbene (NHC) lanthanide amides L 2LnN(TMS)2 (Ln = Y (1), Nd (2), Sm (3), Yb (4)) in 37-40% yields. Molecular structures of 1-4 were determined by X-ray structure analyses. All complexes adopt monomeric structures where each 5-coordinated metal is coordinated by two NHC ligands and one amido group.in distorted trigonal bipyramid geometry. All complexes, especially Yb complex (4), were found to be highly active precatalysts for the catalytic addition of amines to carbodiimides giving guanidines. The system with 4 shows good functional group tolerance and a wide scope of amines including primary and secondary cyclic amines.
- Li, Zhi,Xue, Mingqiang,Yao, Haisheng,Sun, Hongmei,Zhang, Yong,Shen, Qi
-
experimental part
p. 27 - 34
(2012/08/07)
-
- Catalytic guanylation of aliphatic, aromatic, heterocyclic primary and secondary amines using nanocrystalline zinc(II) oxide
-
Nanocrystalline ZnO was found to be a highly efficient heterogeneous catalyst for the guanylation of amines with various carbodiimides to afford N,N′,N″-trisubstituted guanidines in excellent yields. Structurally divergent aliphatic, aromatic, heterocyclic primary and secondary amines were converted to the corresponding N,N′,N″-trisubstituted guanidines using optimal conditions. The catalyst was easy to handle even under atmospheric conditions and can be easily recovered by centrifugation and reused for five cycles with consistent activity.
- Kantam, M. Lakshmi,Priyadarshini,Amal Joseph,Srinivas,Vinu,Klabunde,Nishina, Yuta
-
experimental part
p. 5730 - 5737
(2012/09/08)
-
- Heterobimetallic dianionic guanidinate complexes of lanthanide and lithium: Highly efficient precatalysts for catalytic addition of amines to carbodiimides to synthesize guanidines
-
A series of heterobimetallic dianionic guanidinate complexes of lanthanide and lithium, [Li(THF)(DME)]3Ln[μ- η2η1(iPrN)2C(NC 6H4p-R)]3 [R=Cl, Ln=Nd (I), Y (II), La (III); R=H, Ln=Nd (IV)] were synthesized and fully characterized. These complexes were found to be highly efficient precatalysts for the addition of various primary and secondary amines, and aromatic and aliphatic diamines to carbodiimides to give the corresponding monoguanidine and biguanidine derivatives under mild condition (at 25-60 °C), which provides an efficient way for the synthesis of biguanidines compounds. The activity depends on the central metals and ligands: La>Nd>Y for the metals and [(iPrN) 2C(NC6H4p-Cl)]2->[( iPrN)2C(NC6H5)]2- for the ligands were observed.
- Zhang, Xingmin,Wang, Chuanyong,Qian, Cunwei,Han, Fubin,Xu, Fan,Shen, Qi
-
experimental part
p. 8790 - 8799
(2011/12/02)
-
- Catalytic Depolymerization of Polymers Containing Electrophilic Linkages Using Nucleophilic Reagents
-
The disclosure relates to methods and materials useful for depolymerizing a polymer. In one embodiment, for example, the disclosure provides a method for depolymerizing a polymer containing electrophilic linkages, wherein the method comprises contacting t
- -
-
Page/Page column 11
(2011/01/12)
-
- Acyclic guanidines as organic catalysts for living polymerization of lactide
-
We describe a facile route to structurally diverse guanidinium organic catalysts by reaction of carbodiimides with secondary amines. The efficacy of these catalysts for the living ring-opening polymerization (ROP) of lactide was demonstrated including predictable molecular weights and end-group fidelity. Theoretical studies indicate that the acyclic guanidines are less basic than 1, 5, 7-triazabicyclo[4.4.0]dec-5-ene (TBD), but as for the more active TBD, they catalyze ring opening by activation of the alcohol and by stabilizing the resultant tetrahedral intermediates through hydrogen bonding. These results demonstrate that weak secondary interactions are an important concept for controlled polymerization.
- Zhang, Lei,Pratt, Russell C.,Nederberg, Fredrik,Horn, Hans W.,Rice, Julia E.,Waymouth, Robert M.,Wade, Charles G.,Hedrick, James L.
-
scheme or table
p. 1660 - 1664
(2011/09/20)
-
- Titanacarborane mediated C-N bond forming/breaking reactions
-
Constrained-geometry titanacarboranes [σ:η1:η5-(OCH2)(R2NCH2)C2B9H9]Ti(NR2) (R = Me, Et) are synthesized via an unexpected reaction of [Me3NH][μ-7,8-CH2OCH2-7,8-C2B9H10] with Ti(NR2)4 (R = Me, Et), involving a C-O bond cleavage and C-N bond formation. These complexes can be readily converted to new amide species or alkoxide by reacting with amines or esters, respectively. Insertion of a series of unsaturated molecules into the Ti-N bond of the aforementioned complexes results in the formation of various half-sandwich titanacarboranes. [σ:η1:η5-(OCH2)(Me2NCH2)C2B9H9]Ti(NMe2) is also able to efficiently catalyze the hydroamination of carbodiimides and the transamination of guanidines. These results are summarized in this brief account.
- Shen, Hao,Xie, Zuowei
-
scheme or table
p. 1652 - 1657
(2009/10/11)
-
- Divalent lanthanide complexes: Highly active precatalysts for the addition of N-H and C-H bonds to carbodiimides
-
(Chemical Equation Presented) Various divalent lanthanide complexes with the formula LnL2(sol)x (L = N(TMS)2, sol = THF, x = 3, Ln = Sm (I), Eu (II), Yb (III); L = MeC5H4, sol = THF, x = 2, Ln = Sm (IV); L = ArO(Ar = [2,6-(tBu)2-4- MeC6H2]), sol = THF, x = 2, Ln = Sm (V)), especially complexes I-III, serve as excellent catalyst precursors for catalytic addition of various primary and secondary amines to carbodiimides, efficiently providing the corresponding guanidine derivatives with a wide range of substrates under solvent-free condition. The reaction shows good functional groups tolerence. Complexes I-III are also excellent precatalysts for addition of terminal alkynes to carbodiimides yielding a series of propiolamidines. The active sequence of Yb 5H4 2 for ligand around the metal was observed for both reactions. The first step in both reactions was supposed to include the formation of a bimetallic bisamidinate samarium species originating from the reduction-coupling reaction of carbodiimide promoted by lanthanide(II) complex. The active species is proposed to be a lanthanide guanidinate and a lanthanide amidinate.
- Du, Zhu,Li, Wenbo,Zhu, Xuehua,Xu, Fan,Shen, Qi
-
supporting information; experimental part
p. 8966 - 8972
(2009/04/06)
-
- Synthesis of acylguanidine analogues: inhibitors of ADP-induced platelet aggregation
-
Routine screening of compounds for inhibition of ADP-induced platelet aggregation in vitro revealed that 1'-hexamethylenebis[3-cyclohexyl-3-[(cyclohexylimino)(4-morpholinyl)methyl] urea] was active and represented the first example of a bis(acylguanidine) with possible antithrombotic activity. In order to develop a structure-activity relationship for this class of compounds, we synthesized a number of new bis(acylguanidines). These were tested in vitro, and several analogues were also active. Ex vivo testing revealed that compounds 22, 41, 58, and 70-73 were orally active in rats or guinea pigs.
- Thomas,Nishizawa,Zimmermann,Williams
-
p. 228 - 236
(2007/10/02)
-