An efficient and eco-friendly synthesis of 2-pyridones and functionalized azaxanthone frameworks via indium triflate catalyzed domino reaction

2017 ◽  
Vol 19 (11) ◽  
pp. 2524-2529 ◽  
Author(s):  
N. Poomathi ◽  
P. T. Perumal ◽  
S. Ramakrishna
Keyword(s):  
Environmentally Friendly ◽  
Domino Reaction ◽  
Reusable Catalyst ◽  
One Pot ◽  
Indium Triflate

A green and efficient one-pot method has been developed for the synthesis of 2-pyridone and functionalized azaxanthone frameworks using indium triflate as an environmentally friendly, reusable catalyst.

scholarly journals One-Pot Three-Component Synthesis of 2-Amino-5-oxo-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile Derivatives Catalyzed by Cobalt Doped Iron (III) Tartrate Complex

2021 ◽  
Vol 11 (1) ◽  
pp. 3208-3217
Keyword(s):  
Microwave Irradiation ◽  
Environmentally Friendly ◽  
Water Soluble ◽  
Reusable Catalyst ◽  
Atom Economy ◽  
One Pot ◽  
Hydroxy Coumarin

An environmentally friendly one-pot three-component strategy synthesizing a series of 2-Amino-5-oxo-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile derivatives has been successfully performed in water. The products were obtained through conventional and microwave irradiation, which involving aldehyde, malononitrile, and 4-hydroxy coumarin, resulting in a green synthetic protocol with a high atom economy. The reaction was catalyzed by a water-soluble and reusable catalyst, i.e., cobalt doped iron (III) tartrate complex. The catalyst was recovered and efficiently reused.

scholarly journals Dowex 50W: A Green Mild Reusable Catalyst for the Synthesis of 2-Aryl Benzoxazole Derivatives in Aqueous Medium

2021 ◽  
Vol 37 (2) ◽  
pp. 341-347
Author(s):  
Arup Datta
Keyword(s):  
Aqueous Medium ◽  
Heterogeneous Catalyst ◽  
Environmentally Friendly ◽  
High Yield ◽  
Reusable Catalyst ◽  
One Pot ◽  
Simple Process ◽  
Effective Catalyst ◽  
Rapid Reaction ◽  
Environmentally Friendly Method

In this work simple efficient, one pot and environmentally friendly method was developed for the synthesis of 2-Aryl-1H-benzoxazole derivatives at 80º C using ortho-aminophenol and various aldehydes. It has been found that Dowex50W is an effective catalyst to prepare moderate to high yield of a variety of benzoxazole derivatives through a clean and simple process. Aqueous medium, green methodology, rapid reaction, reusability of heterogeneous catalyst are the great advantages of this protocol.

One-Pot Synthesis of β-Acetamido Ketones Using Aluminum Hydrogen Sulfate as a Reusable Catalyst

2007 ◽  
Vol 4 (7) ◽  
pp. 524-529 ◽  
Author(s):  
Elaheh Mosaddegh ◽  
Mohammad Islami ◽  
Asadollah Hassankhani
Keyword(s):  
Reusable Catalyst ◽  
Hydrogen Sulfate ◽  
One Pot ◽  
One Pot Synthesis

scholarly journals Aqueous one-pot synthesis of well-defined zwitterionic diblock copolymers by RAFT polymerization: an efficient and environmentally-friendly route to a useful dispersant for aqueous pigments

2021 ◽  
Vol 23 (3) ◽  
pp. 1248-1258
Author(s):  
Shannon M. North ◽  
Steven P. Armes
Keyword(s):  
Iron Oxide ◽  
Diblock Copolymers ◽  
Raft Polymerization ◽  
Environmentally Friendly ◽  
Iron Oxide Particles ◽  
One Pot ◽  
One Pot Synthesis ◽  
Highly Effective ◽  
Oxide Particles

An atom-efficient, wholly aqueous one-pot synthesis of zwitterionic diblock copolymers has been devised. Such copolymers can serve as highly effective aqueous dispersants for nano-sized transparent yellow iron oxide particles.

Vegetable oil as a highly effective 100% bio-based alternative solvent for the one-pot multicomponent Biginelli reaction

2021 ◽  
Author(s):  
Pakin Noppawan ◽  
Suwiwat Sangon ◽  
Nontipa Supanchaiyamat ◽  
Andrew J. Hunt
Keyword(s):  
Vegetable Oil ◽  
Palm Oil ◽  
Biginelli Reaction ◽  
Environmentally Friendly ◽  
One Pot ◽  
Highly Effective ◽  
The One ◽  
Biginelli Reactions

Multicomponent one-pot Biginelli reactions have been successfully performed using vegetable oil as bio-based, non-toxic, and environmentally friendly solvents. Palm oil was demonstrated to be a highly effective greener solvent as...

Synthesis of pyrazolo[1,5-c]quinazoline derivatives through the copper-catalyzed domino reaction of o-alkenyl aromatic isocyanides with diazo compounds

2020 ◽  
Vol 56 (55) ◽  
pp. 7665-7668 ◽  
Author(s):  
Lu Liu ◽  
Lei Li ◽  
Shukuan Mao ◽  
Xin Wang ◽  
Ming-Dong Zhou ◽  
...  
Keyword(s):  
Diazo Compounds ◽  
Domino Reaction ◽  
Reaction Conditions ◽  
One Pot ◽  
One Pot Synthesis ◽  
Quinazoline Derivatives

Various o-alkenyl aromatic isocyanides were prepared from readily available reactants for their double annulation with diazo compounds for a one-pot synthesis of pyrazolo[1,5-c]quinazolines under mild reaction conditions.

ChemInform Abstract: A Three-Component Domino Reaction of 2-Tetralone, Hydroxylamine and Acetylene: A One-Pot, Highly Regioselective Synthesis of 4,5-Dihydrobenz[e]indoles.

ChemInform ◽  
2010 ◽  
Vol 41 (28) ◽  
pp. no-no
Author(s):  
Alexander M. Vasil'tsov ◽  
Andrei V. Ivanov ◽  
Al'bina I. Mikhaleva ◽  
Boris A. Trofimov
Keyword(s):  
Regioselective Synthesis ◽  
Domino Reaction ◽  
One Pot
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