Copper‐Catalyzed Asymmetric Arylation of N ‐Heteroaryl Aldimines: Elementary Step of a 1,4‐Insertion

2019 ◽  
Vol 131 (9) ◽  
pp. 2731-2735
Author(s):  
Chunlin Wu ◽  
Xurong Qin ◽  
Adhitya Mangala Putra Moeljadi ◽  
Hajime Hirao ◽  
Jianrong Steve Zhou
Keyword(s):  
Author(s):  
S. F. Lukomskii ◽  
G. S. Berdnikov

We consider a class of (N, M)-elementary step functions on the p-adic Vilenkin group. We prove that (N, M)-elementary step function generates a MRA on p-adic Vilenkin group if and only if it is generated by a special N-valid rooted tree on the set of vertices {0,1,…p - 1} with the vector (0,…,0) ∈ ℤN as a root.


2014 ◽  
Vol 59 (4) ◽  
pp. 1413-1420 ◽  
Author(s):  
K. Pacławski ◽  
J. Piwowonska

Abstract In this work, spectrophotometric studies of the kinetics and mechanism of reaction between [PtCl6]2- complex ions and sodium thiosulfate, were carried out. The influence of different conditions, such as: initial concentrations of reductant and platinum(IV) complex ions, ionic strength, pH and temperature on the rate constant, was experimentally determined. From the obtained results, the molecularity of the first elementary step, value of the enthalpy and entropy of activation in Eyring equation as well as corresponding rate equation, were experimentally determined. It was found that the reaction is relatively slow and leads to the S, Pt and PtS colloids formation. The best conditions for solid phase formation containing Pt are at pH = 5.


2003 ◽  
Vol 42 (17) ◽  
pp. 1932-1935 ◽  
Author(s):  
Jörg Barner ◽  
Frank Mallwitz ◽  
Lijin Shu ◽  
A. Dieter Schlüter ◽  
Jürgen P. Rabe

Desalination ◽  
2002 ◽  
Vol 146 (1-3) ◽  
pp. 41-47 ◽  
Author(s):  
Andre Cornelis van Veen ◽  
David Farrusseng ◽  
Claude Mirodatos

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Xiaotao Zhu ◽  
Wujun Jian ◽  
Meirong Huang ◽  
Daliang Li ◽  
Yajun Li ◽  
...  

AbstractThe straightforward strategy of building a chiral C-O bond directly on a general carbon radical center is challenging and stereocontrol of the reactions of open-chain hydrocarbon radicals remains a largely unsolved problem. Advance in this elementary step will spur the development of asymmetric radical C-O bond construction. Herein, we report a copper-catalyzed regioselective and enantioselective carboesterification of substituted dienes using alkyl diacyl peroxides as the source of both the carbon and oxygen substituents. The participation of external acids in this reaction substantially extends its applicability and leads to structurally diverse allylic ester products. This work represents the advance in the key elementary reaction of intermolecular enantioselective construction of C-O bond on open-chain hydrocarbon radicals and may lead to the discovery of other asymmetric radical reactions.


RSC Advances ◽  
2019 ◽  
Vol 9 (37) ◽  
pp. 21544-21556 ◽  
Author(s):  
Tianlei Zhang ◽  
Yongqi Zhang ◽  
Mingjie Wen ◽  
Zhuo Tang ◽  
Bo Long ◽  
...  

The effects of acidic (FA), neutral (WM) and basic (AM) catalysts on the energetic and kinetic aspects of the HO2 + Cl reaction have been studied. At 298 K, the catalytic order of FA, WM and AM is WM > FA > AM.


2020 ◽  
Vol 49 (5) ◽  
pp. 1487-1516 ◽  
Author(s):  
Tianxiao Jiang ◽  
Haocheng Zhang ◽  
Yongzheng Ding ◽  
Suchen Zou ◽  
Rui Chang ◽  
...  

This review summarizes transition-metal catalyzed reactions with reductive elimination between covalent ligands and dative ligands as the key elementary step.


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