Synthesis of tertiary aryl amines of various aryl halides and secondary amines usingortho-palladated complex of tribenzylamine

2013 ◽  
Vol 27 (12) ◽  
pp. 704-706 ◽  
Author(s):  
Abdol R. Hajipour ◽  
Fatemeh Dordahan ◽  
Fatemeh Rafiee
Keyword(s):  
Aryl Halides ◽  
Secondary Amines ◽  
Aryl Amines

Metal-free green synthesis of aryl amines in magnetized distilled water: experimental aspects and molecular dynamics simulation

2021 ◽  
Author(s):  
Mohammad Bakherad ◽  
Zainab Moosavi-Tekyeh ◽  
Amin Rezaeifard ◽  
Rahele Doosti ◽  
Nasrin Mehmandoost ◽  
...  
Keyword(s):  
Molecular Dynamics ◽  
Molecular Dynamics Simulation ◽  
Transition Metal ◽  
Green Synthesis ◽  
Aryl Halides ◽  
Dynamics Simulation ◽  
Secondary Amines ◽  
Distilled Water ◽  
Metal Free ◽  
Aryl Amines

In this work, a simple, green, and transition metal-free approach to the N-arylation of secondary amines with aryl halides in magnetized distilled water (MDW), as a solvent, is introduced.

d-Glucosamine as a green ligand for copper catalyzed synthesis of primary aryl amines from aryl halides and ammonia

2011 ◽  
Vol 47 (17) ◽  
pp. 5076 ◽  
Author(s):  
Krishna Gopal Thakur ◽  
Dhandapani Ganapathy ◽  
Govindasamy Sekar
Keyword(s):  
Aryl Halides ◽  
Aryl Amines

N-Acyl-N-(4-chlorophenyl)-4-nitrobenzenesulfonamides: highly selective and efficient reagents for acylation of amines in water

2016 ◽  
Vol 71 (2) ◽  
pp. 95-104 ◽  
Author(s):  
Sara Ebrahimi ◽  
Safoura Saiadi ◽  
Simin Dakhilpour ◽  
Seyed Nezamoddin Mirsattari ◽  
Ahmad Reza Massah
Keyword(s):  
High Stability ◽  
Solvent Free ◽  
Secondary Amines ◽  
Primary Amines ◽  
Green Solvent ◽  
One Pot ◽  
Selective Protection ◽  
Solvent Free Conditions ◽  
Aryl Amines ◽  
Acylation Reactions

AbstractA variety ofN-acyl-N-(4-chlorophenyl)-4-nitrobenzenesulfonamides (1a–e) were synthesized in one pot from 4-chloroaniline under solvent-free conditions and have been developed as chemoselective N-acylation reagents. Selective protection of primary amines in the presence of secondary amines, acylation of aliphatic amines in the presence of aryl amines, and monofunctionalization of primary-secondary diamines as well as selective N-acylation of amino alcohols using these reagents are described. All of the acylation reactions were carried out in water as a green solvent. High stability and easy preparation of these acylating reagents are other advantages of this method.

Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides

2016 ◽  
Vol 55 (42) ◽  
pp. 13219-13223 ◽  
Author(s):  
Martins S. Oderinde ◽  
Natalie H. Jones ◽  
Antoine Juneau ◽  
Mathieu Frenette ◽  
Brian Aquila ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Aryl Halides ◽  
Nickel Catalysis ◽  
Aryl Amines ◽  
The Cross

ChemInform Abstract: An Expeditious and Environmentally Benign Preparation of Aryl Halides from Aryl Amines by Solvent-Free Grinding.

ChemInform ◽  
2011 ◽  
Vol 42 (13) ◽  
pp. no-no
Author(s):  
Mi Eun Moon ◽  
Younghwa Choi ◽  
Young Min Lee ◽  
Vaishali Vajpayee ◽  
Marina Trusova ◽  
...  
Keyword(s):  
Solvent Free ◽  
Aryl Halides ◽  
Environmentally Benign ◽  
Aryl Amines

ChemInform Abstract: D-Glucosamine as a Green Ligand for Copper Catalyzed Synthesis of Primary Aryl Amines from Aryl Halides and Ammonia.

ChemInform ◽  
2011 ◽  
Vol 42 (32) ◽  
pp. no-no
Author(s):  
Krishna Gopal Thakur ◽  
Dhandapani Ganapathy ◽  
Govindasamy Sekar
Keyword(s):  
Aryl Halides ◽  
Aryl Amines
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