Literature DB >> 20085353

Efficient one-pot synthesis of spirooxindole derivatives catalyzed by L-proline in aqueous medium.

Yuling Li1, Hui Chen, Chunling Shi, Daqing Shi, Shunjun Ji.   

Abstract

An efficient one-pot synthesis of spirooxindole derivatives by three-component reaction of isatins, malononitrile (cyanoacetic ester) and 1,3-dicarbonyl compounds in water in the presence of l-proline is reported. This new protocol has the advantages of environmental friendliness, higher yields, shorter reaction times, low cost, and convenient operation.

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Year:  2010        PMID: 20085353     DOI: 10.1021/cc9001185

Source DB:  PubMed          Journal:  J Comb Chem        ISSN: 1520-4766


  15 in total

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4.  Caged Proline in Photoinitiated Organocatalysis.

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Review 5.  The molecular diversity scope of 1,3-indandione in organic synthesis.

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7.  CaCl(2) as a bifunctional reusable catalyst: diversity-oriented synthesis of 4H-pyran library under ultrasonic irradiation.

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8.  3',7',7'-Trimethyl-1'-phenyl-5',6',7',8'-tetra-hydro-spiro-[indoline-3,4'-(1H,4H-pyrazolo-[3,4-b]chromene)]-2,5'-dione.

Authors:  Li-Qin Zhao; Bin Li; Yi-Qun Li
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-10

9.  An environmentally benign protocol for aqueous synthesis of tetrahydrobenzo[b]pyrans catalyzed by cost-effective ionic liquid.

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Journal:  Int J Mol Sci       Date:  2014-04-22       Impact factor: 5.923

10.  Synthesis of mono- and bis-spirooxindole derivatives "on water" using double salt of aluminum sulfate-sulfuric acid as a reusable catalyst.

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