Cobalt(II)/N-Hydroxyphthalimide-Catalyzed Cross-Dehydrogenative Coupling Reaction at Room Temperature under Aerobic Condition

2018 ◽  
Vol 83 (8) ◽  
pp. 4477-4490 ◽  
Author(s):  
Mahendra R. Patil ◽  
Noopur P. Dedhia ◽  
Anant R. Kapdi ◽  
A.Vijay Kumar
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Aerobic Condition ◽  
Dehydrogenative Coupling

Copper(ii)-catalyzed cross dehydrogenative coupling reaction of N-hydroxyphthalimide with alkanes and ethers via unactivated C(sp3)–H activation at room temperature

RSC Advances ◽  
2016 ◽  
Vol 6 (82) ◽  
pp. 79016-79019 ◽  
Author(s):  
Zhicheng Guo ◽  
Can Jin ◽  
Jiadi Zhou ◽  
Weike Su
Keyword(s):  
Mild Condition ◽  
Room Temperature ◽  
Reaction System ◽  
Coupling Reaction ◽  
Dehydrogenative Coupling

This reaction system shows mild condition and broad substrate scope for generation of O-substituted N-hydroxyphthalimide derivatives via unactivated C(sp3)–H activation.

Visible Light Mediated Synthesis of Rutaecarpine Alkaloids Through C-N Cross-coupling Reaction

Synlett ◽  
2021 ◽  
Author(s):  
Dong Chen ◽  
Shiqing Li ◽  
Jinhua Wang ◽  
Tiantian Gou ◽  
Linfeng Zhang ◽  
...  
Keyword(s):  
Visible Light ◽  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Hydrogen Phosphate ◽  
Dehydrogenative Coupling ◽  
Cross Coupling Reaction ◽  
Quinazolinone Derivatives ◽  
Electron Donating Groups ◽  
Negligible Influence

A visible-light-initiated cross-dehydrogenative-coupling amination is described, featuring metal- and photocatalyst-free, at room temperature, and using air as an oxidant. The reaction provides a facile approach for the synthesis of rutaecarpine and its derivatives. The substrates with electron-withdrawing groups give higher yields than those with electron-donating groups, but the substituent position has a negligible influence on the yield. Using binaphthyl-diyl hydrogen phosphate and dibenzyl phosphate as catalysts both deliver satisfying yields.This straight-forward light-driven strategy might be applicable to the synthesis of quinazolinone derivatives.

KIO3-catalyzed cross dehydrogenative coupling reaction: sulfenylation of phenol and arylamine derivatives in water at room temperature

2019 ◽  
Vol 17 (4) ◽  
pp. 830-834 ◽  
Author(s):  
Dulin Kong ◽  
Tiao Huang ◽  
Min Liang ◽  
Mingshu Wu ◽  
Qiang Lin
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Metal Free ◽  
Dehydrogenative Coupling

A metal-free direct sulfenylation of phenol and arylamine derivatives with various heterocyclic thiols and thiones using a cross dehydrogenative coupling protocol in water at room temperature has been developed.

Copper-Catalyzed Highly Efficient Esterification of Aldehydes with N-Hydroxyphthalimide via Cross-Dehydrogenative Coupling in Water at Room Temperature

Synlett ◽  
2017 ◽  
Vol 28 (11) ◽  
pp. 1321-1326 ◽  
Author(s):  
Can Jin ◽  
Weike Su ◽  
Zhicheng Guo ◽  
Xinpeng Jiang ◽  
Jiadi Zhou ◽  
...  
Keyword(s):  
Reaction Time ◽  
Efficient Method ◽  
Room Temperature ◽  
Coupling Reaction ◽  
Short Reaction Time ◽  
Mild Conditions ◽  
Highly Efficient ◽  
Dehydrogenative Coupling ◽  
First Time

A copper-catalyzed cross-dehydrogenative coupling reaction between N-hydroxyphthalimide and aldehydes using PhI(OAc)2 as an oxidant is described. It is reported for the first time to synthesize NHPI esters in water, providing the corresponding NHPI esters in moderate to good yields. This facile and efficient method is eco-friendly and possesses the advantages of mild conditions, short reaction time, and broad substrate scope.

scholarly journals Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction

RSC Advances ◽  
2021 ◽  
Vol 11 (14) ◽  
pp. 8051-8054
Author(s):  
Rongxiang Chen ◽  
Bing Liu ◽  
Wenbo Li ◽  
Kai-Kai Wang ◽  
Changqing Miao ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Dehydrogenative Coupling ◽  
Aryl Ketones ◽  
High Yields

A cross dehydrogenative coupling reaction of aryl ketones with N-hydroxyphthalimide was realized. The reactions afforded a clean and facile access to diverse N-alkoxyphthalimide derivatives in high yields (up to 99%).

Hydroxymethylation of quinolines via iron promoted oxidative C–H functionalization: synthesis of arsindoline-A and its derivatives

2021 ◽  
Author(s):  
Bangarigalla Shantharjun ◽  
Damera Vani ◽  
Ramanjaneyulu Unnava ◽  
Mummadi Sandeep ◽  
Kallu Rajender Reddy
Keyword(s):  
Coupling Reaction ◽  
Dehydrogenative Coupling

Herein, we report a mild and efficient hydroxymethylation of quinolines via an iron promoted cross-dehydrogenative coupling reaction under external acid free conditions.

Topology Selectivity in On-Surface Dehydrogenative Coupling Reaction: Dendritic Structure versus Porous Graphene Nanoribbon

ACS Nano ◽  
2021 ◽  
Vol 15 (3) ◽  
pp. 4617-4626
Author(s):  
Jianmin Huang ◽  
Yu Pan ◽  
Tao Wang ◽  
Shengsheng Cui ◽  
Lin Feng ◽  
...  
Keyword(s):  
Dendritic Structure ◽  
Coupling Reaction ◽  
Graphene Nanoribbon ◽  
Porous Graphene ◽  
Dehydrogenative Coupling ◽  
Structure Versus

An Efficient Route to Biaryl Bisbenzocyclobutene Monomers Based on Suzuki Coupling Reaction at Room Temperature.

ChemInform ◽  
2005 ◽  
Vol 36 (38) ◽  
Author(s):  
Jun-xiao Yang ◽  
Kuo-yan Ma ◽  
Fang-hua Zhu ◽  
Wen Chen ◽  
Bo Li ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Suzuki Coupling ◽  
Suzuki Coupling Reaction ◽  
Efficient Route

scholarly journals Eosin Y dye-based porous organic polymers for highly efficient heterogeneous photocatalytic dehydrogenative coupling reaction

RSC Advances ◽  
2017 ◽  
Vol 7 (1) ◽  
pp. 408-414 ◽  
Author(s):  
Chang-An Wang ◽  
Yan-Wei Li ◽  
Xue-Li Cheng ◽  
Jian-Ping Zhang ◽  
Yin-Feng Han
Keyword(s):  
Coupling Reaction ◽  
Eosin Y ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Bottom Up ◽  
Highly Efficient ◽  
Dehydrogenative Coupling ◽  
Highly Effective

Eosin Y dye has been successfully embedded into a nanoporous network EY-POPs through a bottom-up strategy. The polymers could be used as highly effective and reusable heterogeneous organo-photocatalyst for the dehydrogenative coupling reaction.

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