Copper-Catalyzed Oxidative Coupling of Alkenes with Aldehydes: Direct Access to α,β-Unsaturated Ketones

2013 ◽  
Vol 52 (8) ◽  
pp. 2256-2259 ◽  
Author(s):  
Jing Wang ◽  
Chao Liu ◽  
Jiwen Yuan ◽  
Aiwen Lei
Keyword(s):  
Oxidative Coupling ◽  
Direct Access ◽  
Unsaturated Ketones

Copper-Catalyzed Oxidative Coupling of Alkenes with Aldehydes: Direct Access to α,β-Unsaturated Ketones

2013 ◽  
Vol 125 (8) ◽  
pp. 2312-2315 ◽  
Author(s):  
Jing Wang ◽  
Chao Liu ◽  
Jiwen Yuan ◽  
Aiwen Lei
Keyword(s):  
Oxidative Coupling ◽  
Direct Access ◽  
Unsaturated Ketones

ChemInform Abstract: CuBr Catalyzed Aerobic Oxidative Coupling of 2-Aminopyridines with Cinnamaldehydes: Direct Access to 3-Formyl-2-phenyl-imidazo[1,2-a]pyridines.

ChemInform ◽  
2015 ◽  
Vol 46 (49) ◽  
pp. no-no
Author(s):  
Jaideep B. Bharate ◽  
Sheenu Abbat ◽  
Prasad V. Bharatam ◽  
Ram A. Vishwakarma ◽  
Sandip B. Bharate
Keyword(s):  
Oxidative Coupling ◽  
Direct Access

Encapsulating mesoporous metal nanoparticles: towards a highly active and stable nanoreactor for oxidative coupling reactions in water

2019 ◽  
Vol 55 (42) ◽  
pp. 5898-5901 ◽  
Author(s):  
Houbing Zou ◽  
Jinyu Dai ◽  
Runwei Wang
Keyword(s):  
Metal Nanoparticles ◽  
Oxidative Coupling ◽  
Coupling Reaction ◽  
Efficient Production ◽  
Coupling Reactions ◽  
One Pot ◽  
Unsaturated Ketones ◽  
Oxidative Coupling Reaction ◽  
Highly Active ◽  
Mesoporous Metal

We design and prepare a highly active and stable nanoreactor by encapsulating mesoporous metal nanoparticles for efficient production of α,β-unsaturated ketones via a one-pot oxidative coupling reaction.

Modular DNA-based hybrid catalysts as a toolbox for enantioselective hydration of α,β-unsaturated ketones

2019 ◽  
Vol 17 (9) ◽  
pp. 2548-2553 ◽  
Author(s):  
Ji Hye Yum ◽  
Soyoung Park ◽  
Ryota Hiraga ◽  
Izumi Okamura ◽  
Shunta Notsu ◽  
...  
Keyword(s):  
Double Bond ◽  
Direct Access ◽  
Chiral Alcohols ◽  
Unsaturated Ketones ◽  
Hybrid Catalysts ◽  
Carbon Double Bond ◽  
Direct Addition

The direct addition of water to a carbon–carbon double bond remains a challenge, but such a reaction is essential for the development of efficient catalysts that enable direct access to chiral alcohols.

Copper-catalyzed aerobic oxidative coupling of o-phenylenediamines with 2-aryl/heteroarylethylamines: direct access to construct quinoxalines

2017 ◽  
Vol 15 (10) ◽  
pp. 2259-2268 ◽  
Author(s):  
Kovuru Gopalaiah ◽  
Anupama Saini ◽  
Sankala Naga Chandrudu ◽  
Devarapalli Chenna Rao ◽  
Harsh Yadav ◽  
...  
Keyword(s):  
Oxidative Coupling ◽  
Direct Access

A versatile method for synthesis of quinoxalines by Cu-catalyzed oxidative coupling of o-phenylenediamines with 2-arylethylamines is presented.

scholarly journals Alternative pathways to α,β-unsaturated ketones via direct oxidative coupling transformation using Sr-doped LaCoO 3 perovskite catalyst

2019 ◽  
Vol 6 (11) ◽  
pp. 191313
Author(s):  
Khang H. Trinh ◽  
Son H. Doan ◽  
Tien V. Huynh ◽  
Phuong H. Tran ◽  
Diep N. Pham ◽  
...  
Keyword(s):  
Oxidative Coupling ◽  
Coupling Reaction ◽  
Aromatic Aldehydes ◽  
Alternative Pathways ◽  
Unsaturated Ketones ◽  
Dibenzyl Ether ◽  
Oxidative Coupling Reaction ◽  
Coupling Transformation ◽  
Perovskite Material ◽  
High Yields

A strontium-doped lanthanum cobaltite perovskite material was prepared, and used as a recyclable and effective heterogeneous catalyst for the direct oxidative coupling of alkenes with aromatic aldehydes to produce α,β-unsaturated ketones. The reaction afforded high yields in the presence of di- tert -butylperoxide as oxidant. Single oxides or salts of strontium, lanthanum and cobalt, and the undoped perovskite offered a lower catalytic activity than the strontium-doped perovskite. Benzaldehyde could be replaced by benzyl alcohol, dibenzyl ether, 2-oxo-2-phenylacetaldehyde, 2-bromoacetophenone or (dimethoxymethyl) benzene in the oxidative coupling reaction with alkenes. To our best knowledge, reactions between these starting materials with alkenes are new and unknown in the literature.

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