Modulating Two Copper(I)-Catalyzed Orthogonal “Click” Reactions for the One-Pot Synthesis of Highly Branched Polymer Architectures at 25 °C

2011 ◽  
Vol 44 (12) ◽  
pp. 4814-4827 ◽  
Author(s):  
Craig A. Bell ◽  
Zhongfan Jia ◽  
Jakov Kulis ◽  
Michael J. Monteiro
Keyword(s):  
One Pot ◽  
Branched Polymer ◽  
Click Reactions ◽  
One Pot Synthesis ◽  
Polymer Architectures ◽  
The One

Combining Click Reactions for the One-Pot Synthesis of Modular Biomolecule Mimetics

2019 ◽  
Vol 21 (18) ◽  
pp. 7544-7548 ◽  
Author(s):  
Anne Brinkø ◽  
Christian Risinger ◽  
Annie Lambert ◽  
Ola Blixt ◽  
Cyrille Grandjean ◽  
...  
Keyword(s):  
One Pot ◽  
Click Reactions ◽  
One Pot Synthesis ◽  
The One

An Overview of the One-pot Synthesis of Imidazolines

2020 ◽  
Vol 24 (20) ◽  
pp. 2341-2355
Author(s):  
Thaipparambil Aneeja ◽  
Sankaran Radhika ◽  
Mohan Neetha ◽  
Gopinathan Anilkumar
Keyword(s):  
Asymmetric Catalysis ◽  
Organic Compounds ◽  
Ring Opening ◽  
Ecological Impact ◽  
Chiral Auxiliary ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One ◽  
Synthetic Intermediate ◽  
Heterocyclic Moiety

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.

Convenient One-Pot Synthesis of α-Selenonitriles, α-Selenoesters and Asymmetrical Selenides by a Sm/ZnCl2 system in DMF-H2O

2001 ◽  
Vol 2001 (4) ◽  
pp. 160-161 ◽  
Author(s):  
Hongyun Guo ◽  
Yunfa Zheng ◽  
Yongmin Zhang
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Organic Halides ◽  
The One

α-Selenonitriles, α-selenoesters, and asymmetrical selenides can be readily obtained from the one-pot reaction of diselenides and active organic halides by a Sm/ZnCl2 system in DMF-H2O.

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