Facile fabrication of triphenylamine-based conjugated porous polymers and their application in organic degradation under visible light

2020 ◽  
Vol 44 (7) ◽  
pp. 2986-2995 ◽  
Author(s):  
Lidan Lan ◽  
Fei Liu ◽  
Yi Dan ◽  
Long Jiang
Keyword(s):  
Schiff Base ◽  
Visible Light ◽  
Porous Polymers ◽  
Fabrication Method ◽  
Ambient Conditions ◽  
One Pot ◽  
Organic Degradation ◽  
One Pot Synthesis ◽  
Facile Fabrication ◽  
The One

A facile fabrication method was developed for the one-pot synthesis of 1,3,5-triformylbenzene (TFB)-4,4′4′′-triaminotriphenylamine (TPA) and 1,3,5-triformylbenzene-terephthalaldehyde (TA) under ambient conditions via a Schiff-base reaction.

Visible light active CdS nanorods: one-pot synthesis of aldonitrones

2016 ◽  
Vol 40 (11) ◽  
pp. 9257-9262 ◽  
Author(s):  
Moosa Ramdar ◽  
Foad Kazemi ◽  
Babak Kaboudin ◽  
Zahra Taran ◽  
Adel Partovi
Keyword(s):  
Visible Light ◽  
One Pot ◽  
Blue Led ◽  
One Pot Synthesis ◽  
Cds Nanorods ◽  
Visible Light Active ◽  
The One ◽  
Led Irradiation

A new CdS nanorod was synthesized and it was used in the one-pot synthesis of aldonitrones under blue LED irradiation.

Palladium Nanoparticles Catalyzed Synthesis of Benzofurans by a Domino Approach

Synthesis ◽  
2015 ◽  
Vol 47 (11) ◽  
pp. 1661-1668 ◽  
Author(s):  
Pavan Mandali ◽  
Dillip Chand
Keyword(s):  
Palladium Nanoparticles ◽  
Cross Coupling ◽  
Significant Loss ◽  
Coupling Reactions ◽  
Ambient Conditions ◽  
One Pot ◽  
One Pot Synthesis ◽  
Cross Coupling Reactions ◽  
The One

Palladium nanoparticles (PdNPs) were used as a catalyst for the one-pot synthesis of a variety of benzofurans by Sonogashira cross-coupling reactions under ambient conditions. The catalyst could be recycled without significant loss in its activity.

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.

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