scholarly journals Mechanistic Insights into the One-Pot Synthesis of Propargylamines from Terminal Alkynes and Amines in Chlorinated Solvents Catalyzed by Gold Compounds and Nanoparticles

2010 ◽  
Vol 16 (30) ◽  
pp. 9287-9296 ◽  
Author(s):  
David Aguilar ◽  
Maria Contel ◽  
Esteban P. Urriolabeitia
Author(s):  
Guguloth Veeranna ◽  
Ramesh Balaboina ◽  
Narasimha Swamy Thirukovela ◽  
Ravindhar Vadde

The one-pot three-component reaction of several 2-ketoaldehdyes, secondary amines and terminal alkynes to access 3-aminofurans was proceeded well in [bmim][PF6] using a simple and cheap CuI catalyst. The resulted 3-aminofuran...


2007 ◽  
Vol 9 (19) ◽  
pp. 3737-3740 ◽  
Author(s):  
Bruce H. Lipshutz ◽  
Tom Butler ◽  
Asher Lower ◽  
Jeff Servesko

2015 ◽  
Vol 19 (11) ◽  
pp. 1544-1547 ◽  
Author(s):  
Sebastian A. Löw ◽  
Bettina M. Nestl ◽  
Martin J. Weissenborn ◽  
Ferdinand Zepeck ◽  
Bernhard Hauer

2020 ◽  
Vol 24 (20) ◽  
pp. 2341-2355
Author(s):  
Thaipparambil Aneeja ◽  
Sankaran Radhika ◽  
Mohan Neetha ◽  
Gopinathan Anilkumar

One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.


Sign in / Sign up

Export Citation Format

Share Document