scholarly journals Integration of a Nucleoside triphosphate regeneration system in the one‐pot synthesis of UDP‐sugars and hyaluronic acid

ChemCatChem ◽  
2021 ◽  
Author(s):  
Johannes Gottschalk ◽  
Lea Blaschke ◽  
Miriam Aßmann ◽  
Jürgen Kuballa ◽  
Lothar Elling
Keyword(s):  
Hyaluronic Acid ◽  
Nucleoside Triphosphate ◽  
Regeneration System ◽  
One Pot ◽  
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.

The “one pot” synthesis of 4,5-dihydrobenzo[g]indole and its 1-vinyl derivative from 1-tetralone, hydroxylamine, and dichloroethane in the system KOH-DMSO

2013 ◽  
Vol 62 (11) ◽  
pp. 2557-2558 ◽  
Author(s):  
A. V. Ivanov ◽  
V. S. Barnakova ◽  
A. I. Mikhaleva ◽  
B. A. Trofimov
Keyword(s):  
One Pot ◽  
Vinyl Derivative ◽  
One Pot Synthesis ◽  
The One

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.

A New Strategy for the One Pot Synthesis of (Aryloxyimino)Ethylcoumarins Promoted by CuCl2

2012 ◽  
Vol 36 (1) ◽  
pp. 5-8 ◽  
Author(s):  
Gargi Pal ◽  
Pranabes Bhattacharyya ◽  
Arunima Medda ◽  
Asish R. Das
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
New Strategy ◽  
The One
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