scholarly journals Manganese Catalysed Dehydrogenative Synthesis of Urea Derivatives and Polyureas

Author(s):  
Aniekan Owen ◽  
Annika Preiss ◽  
Angus McLuskie ◽  
Chang Gao ◽  
Gavin Peters ◽  
...  

Urea derivatives are prevalent intermediates in the synthesis of resin precursors, dyes, agrochemicals, and pharmaceutical drugs. Furthermore, polyureas are useful plastics with applications in coating, adhesive, and biomedical industries and have a current annual market of USD 885 million. However, the conventional methods for the synthesis of urea derivatives and polyureas involve toxic reagents such as (di)isocyanates, phosgene, CO, and azides. We present here the synthesis of (poly)ureas using much less toxic reagents - (di)amines, and methanol via a catalytic dehydrogenative coupling process. The reaction is catalyzed by a pincer complex of an earth-abundant metal, manganese, and liberates H2 gas, valuable by itself, as the only by-product making the overall process atom-economic, and sustainable. A broad variety of symmetrical, and unsymmetrical urea derivatives and polyureas have been synthesized in moderate to quantitative yields using this catalytic protocol. Mechanistic insights have also been provided using experiments and DFT computation suggesting that the reaction proceeds via an isocyanate intermediate.

2018 ◽  
Vol 8 (14) ◽  
pp. 3469-3473 ◽  
Author(s):  
Siba P. Midya ◽  
Jayaraman Pitchaimani ◽  
Vinod G. Landge ◽  
Vedichi Madhu ◽  
Ekambaram Balaraman

A Co(ii)-NNN pincer complex catalyzed directN-alkylation of anilines with alcoholsviahydrogen auto-transfer and selective acceptorless dehydrogenative coupling of benzylamines with alcohols affording imines with the liberation of molecular hydrogen and water is reported.


2020 ◽  
Vol 22 (10) ◽  
pp. 3079-3082 ◽  
Author(s):  
Uttam Kumar Das ◽  
Trevor Janes ◽  
Amit Kumar ◽  
David Milstein

Herein we report the selective hydrogenation of cyclic imides to diols and amines, homogeneously catalyzed for the first time by a complex of an earth-abundant metal, a manganese pincer complex.


2017 ◽  
Vol 56 (47) ◽  
pp. 14992-14996 ◽  
Author(s):  
Amit Kumar ◽  
Noel Angel Espinosa-Jalapa ◽  
Gregory Leitus ◽  
Yael Diskin-Posner ◽  
Liat Avram ◽  
...  

2021 ◽  
Author(s):  
Jun Chen ◽  
Yu-Jie Liang ◽  
Peng-Zi Wang ◽  
Guo-Qing Li ◽  
Bin Zhang ◽  
...  

<b>Whereas considerable advances have recently been achieved in radical-involved catalytic asymmetric C-N bond formation, there has been little progress in the corresponding C-O bond-forming processes. Here we describe a photoinduced copper-catalyzed cross-coupling of readily oxime esters and 1,3-dienes to generate diversely substituted allylic esters with high regio- and enantioselectivity (>75 examples; up to 95% ee). The reaction proceeds at room temperature under excitation by purple light-emitting diodes and features the use of a single, earth-abundant copper-based chiral catalyst as both the photoredox catalyst for radical generation and the source of asymmetric induction in C-O coupling. Combined experimental and DFT computational studies suggest the formation of π-allylcopper complex from redox-active oxime esters as bifunctional reagents and 1,3-dienes through a radical-polar crossover process.</b>


2019 ◽  
Vol 43 (19) ◽  
pp. 7403-7408 ◽  
Author(s):  
Kishor D. Mane ◽  
Rohit B. Kamble ◽  
Gurunath Suryavanshi

The white light mediated, 3C alkylation of quinoxalin-2(1H)-ones via a cross dehydrogenative coupling (CDC) reaction with cyclic ethers using eosin Y as a photocatalyst is described. The reaction proceeds via a hydrogen abstraction and transfer process.


2018 ◽  
Vol 16 (2) ◽  
pp. 274-284 ◽  
Author(s):  
Seuli Parua ◽  
Rina Sikari ◽  
Suman Sinha ◽  
Siuli Das ◽  
Gargi Chakraborty ◽  
...  

A general, efficient and environmentally benign, one-step synthesis of substituted quinoline derivatives was achieved by acceptorless dehydrogenative coupling of o-aminobenzylalcohols with ketones and secondary alcohols catalyzed by a cheap, earth abundant and easy to prepare macrocyclic nickel catalyst [Ni(MeTAA)].


2019 ◽  
Vol 944 ◽  
pp. 643-649
Author(s):  
Ka Wang ◽  
Hai Zeng Song ◽  
Wei Lan Guo ◽  
Shan Cheng Yan

In response to global energy and environmental issues, development of efficient and robust earth-abundant electrocatalysts for hydrogen evolution reaction is particularly meaningful. In this study, a facile hydrothermal method is developed to synthesize porous CoS2 nanostructures by using sulfur powder and thiourea as sulfur sources on carbon cloths for highly efficient hydrogen evolution reactions. The huge load of CoS2 on carbon cloth,their unique porous nanostructures equiped CoS2 nanomaterials with excellent electrocatalytic properties. The remarkable HER catalytic performance was achieved with -67 mV at a current density -10 mA cm-2 and the Tafel slope 62 mV dec-1 in 0.5 M H2SO4 solution. The overpotential of HER only lost 2 mV after 1000 cycles with remarkable stability. I think this work opens up a low cost and scalable route to fabricate transition metal-based materials for application in electrocatalysis.


2017 ◽  
Vol 139 (34) ◽  
pp. 11722-11725 ◽  
Author(s):  
Noel Angel Espinosa-Jalapa ◽  
Amit Kumar ◽  
Gregory Leitus ◽  
Yael Diskin-Posner ◽  
David Milstein

2022 ◽  
Author(s):  
Chandra Volla ◽  
Arnab Dey ◽  
Anurag Singh

An efficient oxidative [3+2] annulation reaction of aryl hydrazones and heterobicyclic alkenes has been realized with inexpensive and earth-abundant cobalt-salts under aerobic conditions. The reaction proceeds via directing-group assisted C-H...


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