منابع مشابه
Aqua mediated SnO2 nanoparticles: A recyclable and benign catalyst for the synthesis of Quinoxalines
An efficient and mild synthesis of quinoxalines in cludingcyclo-condensation of 1, 2-phenylenediamine and 1, 2-diketonesin the presence of1mol% catalytic amount of SnO2 nanoparticles (1 mol%) in water at room temperature is established. On the whole, this study introduced at this point is substantial in terms of using water as solvent, low reaction time (5 to 10 minutes), high yields...
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The reaction of 3-mercaptopropylsilica (MPS) and chlorosulfonic acid in chloroform afforded silica bonded S-sulfonic acid (SBSSA), which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be recycled and reused several times without any loss of efficiency.
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چکیده ندارد.
Metal catalyst free cyclization of 3-alkynyl substituted 2-(indol-3-yl)quinoxalines in TFA alone: a new synthesis of indolophenazines.
TFA alone was found to be remarkably effective for the intramolecular hydroarylation (IMHA) of alkynes when employed as a solvent in the cyclization of 3-alkynyl substituted 2-(indol-3-yl)quinoxalines. This simple and metal free cyclization method afforded a range of indolophenazines as new and potential cytotoxic agents. The use of excess TFA was found to be crucial for the success of this rea...
متن کاملA mild, catalyst-free synthesis of 2-aminopyridines.
Alkylation of 2-mercaptopyridine with 1,2-dibromoethane affords a cyclic dihydrothiazolopyridinium salt that can serve as a precursor of 2-aminopyridines. Its reaction with primary or secondary amines, either neat or in DMSO, under mild conditions gives the title compounds.
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ژورنال
عنوان ژورنال: Asian Journal of Chemistry
سال: 2015
ISSN: 0970-7077,0975-427X
DOI: 10.14233/ajchem.2015.18680