One-pot Green Synthesis of 3-Methyl-4-aryl-2,4,5,7-tetrahydropyrazolo[3,4-b]pyridine-6-ones by Multicomponent Assembling of 5-Methylpyrazol-3-amine, Aldehydes, and Meldrum's Acid Using Sodium Dodecyl Sulfate (SDS) in Water

2016 ◽  
Vol 54 (2) ◽  
pp. 1640-1644 ◽  
Author(s):  
Saba Hemmati ◽  
Parisa Safarimehr ◽  
Maryam Safaei ◽  
Malak Hekmati
Keyword(s):  
Sodium Dodecyl Sulfate ◽  
Green Synthesis ◽  
Sodium Dodecyl ◽  
Meldrum's Acid ◽  
Meldrum’S Acid ◽  
One Pot ◽  
Dodecyl Sulfate

Green synthesis of gold nanoparticles reduced and stabilized by sodium glutamate and sodium dodecyl sulfate

2017 ◽  
Vol 484 (4) ◽  
pp. 774-780 ◽  
Author(s):  
Gil Felicisimo S. Cabrera ◽  
Michelle M. Balbin ◽  
Paul John G. Eugenio ◽  
Charleo S. Zapanta ◽  
Juvy J. Monserate ◽  
...  
Keyword(s):  
Gold Nanoparticles ◽  
Sodium Dodecyl Sulfate ◽  
Green Synthesis ◽  
Sodium Dodecyl ◽  
Sodium Glutamate ◽  
Dodecyl Sulfate

Sodium Dodecyl Sulfate-assisted Synthesis of 1-(Benzothiazolylamino)methyl-2-naphthols in Water

2010 ◽  
Vol 63 (11) ◽  
pp. 1538 ◽  
Author(s):  
Anil Kumar ◽  
M. Sudershan Rao ◽  
V. Kameswara Rao
Keyword(s):  
Reaction Time ◽  
Sodium Dodecyl Sulfate ◽  
Sodium Dodecyl ◽  
Efficient Synthesis ◽  
One Pot ◽  
Short Reaction Time ◽  
One Pot Condensation ◽  
Dodecyl Sulfate

An efficient synthesis of 1‐(benzothiazolylamino)methyl‐2‐naphthols has been developed in water by one‐pot condensation of 2‐naphthol, aldehydes and 2‐aminobenzothiazole catalyzed by sodium dodecyl sulfate. Advantages of the methodology include a very short reaction time, excellent yields and catalytic use of the sodium dodecyl sulfate.

scholarly journals Green synthesis of new chiral 1-(arylamino)imidazo[2,1-a]isoindole-2,5-diones from the corresponding α-amino acid arylhydrazides in aqueous medium

2018 ◽  
Vol 14 ◽  
pp. 2923-2930 ◽  
Author(s):  
Nadia Bouzayani ◽  
Jamil Kraїem ◽  
Sylvain Marque ◽  
Yakdhane Kacem ◽  
Abel Carlin-Sinclair ◽  
...  
Keyword(s):  
Amino Acid ◽  
Sodium Dodecyl Sulfate ◽  
Green Synthesis ◽  
Aqueous Medium ◽  
Sodium Dodecyl ◽  
Tricyclic Core ◽  
Dodecyl Sulfate

New chiral 1-(arylamino)imidazo[2,1-a]isoindole-2,5-dione derivatives were obtained in good to excellent yields via the cyclocondensation of 2-formylbenzoic acid and various α-amino acid arylhydrazides using water as the solvent in the presence of sodium dodecyl sulfate as the surfactant and under simple and minimum manipulation, without purification. The reaction is totally diastereoselective and gives access to the nitrogenated tricyclic core with a relative trans stereochemistry.

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