Zn-Proline Catalyzed Selective Synthesis of 1,2-Disubstituted Benzimidazoles in Water
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概要
- 論文の詳細を見る
Zn-proline (5 mol%) performs as a novel water-soluble and recyclable Lewis acid catalyst for the selective synthesis of 1,2-disubstituted benzimidazoles from wide range of substituted o-phenylenediamines and aldehydes in moderate to excellent isolated yields (42-92%) using water as solvent at ambient temperature.
- 公益社団法人日本薬学会の論文
- 2007-08-01
著者
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Ramu Enugala
Indian Institute Of Chemical Technology
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RAVI Varala
Indian Institute of Chemical Technology
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VIJAY Kotra
Indian Institute of Chemical Technology
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SRINIVAS RAO
Indian Institute of Chemical Technology
関連論文
- CsOH・H_2O Promoted Areneselenenylation of Aryl Bromides and Iodides
- Zn-Proline Catalyzed Selective Synthesis of 1,2-Disubstituted Benzimidazoles in Water