A green procedure for the synthesis of 1,8-dioxodecahydroacridine derivatives under microwave irradiation in aqueous media without catalyst

2010 ◽  
pp. NA-NA ◽  
Author(s):  
Zi-Qiang Tang ◽  
Yan Chen ◽  
Chang-Ning Liu ◽  
Ke-Ying Cai ◽  
Shu-Jiang Tu
Keyword(s):  
Microwave Irradiation ◽  
Aqueous Media ◽  
Green Procedure

ChemInform Abstract: A Green Procedure for the Synthesis of 1,8-Dioxodecahydroacridine Derivatives under Microwave Irradiation in Aqueous Media Without Catalyst.

ChemInform ◽  
2010 ◽  
Vol 41 (34) ◽  
pp. no-no
Author(s):  
Zi-Qiang Tang ◽  
Yan Chen ◽  
Chang-Ning Liu ◽  
Ke-Ying Cai ◽  
Shu-Jiang Tu
Keyword(s):  
Microwave Irradiation ◽  
Aqueous Media ◽  
Green Procedure

Fast and Efficient Green Procedure for the Synthesis of Benzo[5,6]chromene Derivatives and Their Sulfur Analogues in Water by Organocatalyst Potassium Phthalimide-N-oxyl

Synthesis ◽  
2020 ◽  
Vol 52 (11) ◽  
pp. 1707-1718
Author(s):  
Nasser Etivand ◽  
Jabbar Khalafy ◽  
Mohammad G. Dekamin
Keyword(s):  
Aqueous Media ◽  
Thiobarbituric Acid ◽  
Environmentally Benign ◽  
The Novel ◽  
One Pot ◽  
Synthetic Strategy ◽  
Three Component Reaction ◽  
High Yields ◽  
Green Procedure ◽  
Arylglyoxal Monohydrates

A simple, clean, straightforward, and environmentally benign one-pot, three-component reaction of various arylglyoxal monohydrates, β-naphthol, and barbituric acid [pyrimidine-2,4,6(1H,3H,5H)-trione] or thiobarbituric acid in the presence of catalytic amounts potassium phthalimide-N-oxyl (PPINO), as a mild and efficient organocatalyst in aqueous media under reflux conditions is reported. This transformation produced the novel diverse-substituted 12-benzoyl-8,12-dihydro-9H-benzo[5,6]chromeno[2,3-d]pyrimidine-9,11(10H)-diones and their sulfur analogues in 82–93% yield via filtration and without utilization of any chromatography. The high yields of products, very simple operation, easy workup, availability of starting materials, green process, and high atom-economy are the main benefits of this synthetic strategy.

A Mild, Efficient, and Green Procedure for Michael Addition of Active Methylene Compounds to Chalcones Under Microwave Irradiation

2005 ◽  
Vol 35 (2) ◽  
pp. 325-332 ◽  
Author(s):  
Satya Paul ◽  
Monika Gupta ◽  
Parvinder Pal Singh ◽  
Rajive Gupta ◽  
André Loupy
Keyword(s):  
Microwave Irradiation ◽  
Michael Addition ◽  
Active Methylene Compounds ◽  
Green Procedure ◽  
Active Methylene

A catalytic and green procedure for Friedlander quinoline synthesis in aqueous media

2007 ◽  
Vol 8 (8) ◽  
pp. 1214-1218 ◽  
Author(s):  
Mohammad Ali Zolfigol ◽  
Peyman Salehi ◽  
Arash Ghaderi ◽  
Morteza Shiri
Keyword(s):  
Aqueous Media ◽  
Green Procedure

The Novel SO3H-Functionalized Ionic Liquids Promoted Synthesis of Xanthenedione Derivatives in Aqueous Media under Microwave Irradiation

2011 ◽  
Vol 391-392 ◽  
pp. 1354-1357 ◽  
Author(s):  
Bai Lin Li ◽  
Hua Ding Liang ◽  
Ai Guo Zhong ◽  
Dan Qian Xu
Keyword(s):  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Organic Solvents ◽  
Catalytic System ◽  
Aqueous Media ◽  
Environmentally Friendly ◽  
Separation Process ◽  
The Novel ◽  
Simple Operation

Novel SO3H-functionalized ionic liquids were successfully applied as catalysts for synthesis of xanthenediones under microwave irradiation in Aqueous. Various types of Xanthenes were provided in 90-97% yields using the catalytic system of [(HSO3-p)2im][CF3SO3]/H2O. The products could be conveniently separated from the reaction mixture by filtration and the dissolved catalyst could be reused without any treatment, which of the separation process was performed in water without using any organic solvents. The method not only has the adventages of shrot time and simple operation, but also is environmentally friendly.

A practical and rapid synthesis of 2-aryloxymethylene-6-arylimidazo [2,1-b][1,3,4]thiadiazole in aqueous media

2005 ◽  
Vol 2005 (11) ◽  
pp. 744-746 ◽  
Author(s):  
Xi-Cun Wang ◽  
Man-Gang Wang ◽  
Zhi Yang ◽  
Zheng-Jun Quan ◽  
Fang Wang ◽  
...  
Keyword(s):  
Microwave Irradiation ◽  
Condensation Reaction ◽  
Aqueous Media ◽  
Rapid Synthesis ◽  
Rapid Procedure

A practical and rapid procedure is reported for the synthesis of a variety of 2-aryloxymethylene-6-arylimidazo[2,1-b][1,3,4]thiadiazole 3a–m by condensation reaction of 2-amino-5-aryloxymethylene-1,3,4-thiadiazole 1a–g with ω-bromoacetophenone derivatives 2a–b in aqueous media under microwave irradiation and yielded a series of novel compounds. The procedure is simple and the yields are good to excellent.

Microwave-assisted regioselective synthesis of acyclic nucleosides through an alkylating reaction with 2-oxa-1,4-butanediol diacetate

2006 ◽  
Vol 84 (5) ◽  
pp. 819-824 ◽  
Author(s):  
Guirong Qu ◽  
Suhui Han ◽  
Zhiguang Zhang ◽  
Mingwei Geng ◽  
Feng Xue
Keyword(s):  
Reaction Time ◽  
Microwave Irradiation ◽  
Regioselective Synthesis ◽  
Environmental Friendliness ◽  
Short Reaction Time ◽  
Microwave Assisted ◽  
Acyclic Nucleosides ◽  
Green Procedure ◽  
Simple Manipulation

An efficient and green procedure for the synthesis of purine acyclic nucleosides through microwave-assisted alkylation of various purine nucleobases with 2-oxa-1,4-butanediol diacetate in the absence of solvent and catalyst is described. The advantages of using this method include its environmental friendliness, simple manipulation, short reaction time, high regioselectivity, and good yields.Key words: acyclic nucleosides, microwave irradiation, regioselectivity, alkylation, 2-oxa-1,4-butanediol diacetate.

An operationally simple green procedure for the synthesis of dihydropyrimido[4,5-d]pyrimidinetriones using CuI nanoparticles as a highly efficient catalyst

2015 ◽  
Vol 70 (3) ◽  
pp. 171-176 ◽  
Author(s):  
Shahrzad Abdolmohammadi ◽  
Maryam Afsharpour
Keyword(s):  
Room Temperature ◽  
Aqueous Media ◽  
Coupling Reaction ◽  
Aromatic Aldehydes ◽  
Significant Loss ◽  
Efficient Catalyst ◽  
Nano Crystalline ◽  
Simple Protocol ◽  
High Yields ◽  
Green Procedure

AbstractA green, efficient and simple protocol was developed for the synthesis of dihydropyrimido[4,5-d]pyrimidinetrione derivatives via a coupling reaction of 6-aminouracils, aromatic aldehydes and urea in aqueous media in the presence of nano-crystalline CuI at room temperature. The products were obtained in high yields. CuI nanoparticles can be recycled three times without significant loss of catalytic activity.

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