ChemInform Abstract: Catalytic Cyanation of Carbon-Carbon Triple Bonds Through a Three-Component Cross-Coupling Reaction under Nickel Catalysis.

ChemInform ◽  
2014 ◽  
Vol 45 (14) ◽  
pp. no-no
Author(s):  
Xiaofei Yang ◽  
Shigeru Arai ◽  
Atsushi Nishida
2019 ◽  
Vol 25 (35) ◽  
pp. 8371-8386 ◽  
Author(s):  
Irene Erdelmeier ◽  
Gerd Bülow ◽  
Chang‐Wan Woo ◽  
Jürgen Decker ◽  
Gerhard Raabe ◽  
...  

2019 ◽  
Vol 55 (97) ◽  
pp. 14657-14660 ◽  
Author(s):  
Yingying Ma ◽  
Shihui Liu ◽  
Yifan Xi ◽  
Hongrui Li ◽  
Kai Yang ◽  
...  

A photoredox/nickel dual-catalyzed decarboxylative cross-coupling reaction of anomeric ribosyl/deoxyribosyl acids with aryl/heteroaryl bromides has been developed.


2018 ◽  
Vol 5 (21) ◽  
pp. 3098-3102 ◽  
Author(s):  
Quan-Quan Zhou ◽  
Fu-Dong Lu ◽  
Dan Liu ◽  
Liang-Qiu Lu ◽  
Wen-Jing Xiao

Chiral 2,2′-bipyridine ligands are key to success in an enantioselective desymmetric C–O cross coupling reaction via dual visible light photoredox and nickel catalysis, resulting in chiral 1,4-benzodioxanes under mild reaction conditions.


2013 ◽  
Vol 125 (31) ◽  
pp. 8305-8308 ◽  
Author(s):  
Shigeru Arai ◽  
Yuka Amako ◽  
Xiaofei Yang ◽  
Atsushi Nishida

2020 ◽  
Author(s):  
Evgeny Tretyakov ◽  
Svetlana Zhivetyeva ◽  
Pavel Petunin ◽  
Dmitry Gorbunov ◽  
Nina Gritsan ◽  
...  

<p>Verdazyl-nitroxide diradicals were synthesized using the palladium-catalyzed cross-coupling reaction of the corresponding iodoverdazyls with a nitronyl nitroxide-2-ide gold(I) complex with high yields (up to 82%). The synthesized diradicals were found to be highly thermally stable and have a singlet (D<i>E</i><sub>ST</sub> » -64 cm<sup>–1</sup>) or triplet ground state (D<i>E</i><sub>ST</sub> ³ 25 and 100 cm<sup>–1</sup>), depending on which canonical hydrocarbon diradical type they belong to. Upon crystallization, triplet diradicals form unique one-dimensional (1D) spin <i>S</i> = 1 chains of organic diradicals with intrachain ferromagnetic coupling of <i>J</i>′/<i>k</i><sub>B</sub> from 3 to 6 K.</p>


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