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Lewis Acid Catalyzed One-Pot Selective Synthesis of Aminobenzofurans and N-Alkyl-2-aryl-2-(arylimino)acetamides: Product Dependence on the Nature of the Aniline
EPrints@IICB
View Archive Info| Field | Value | |
| Title |
Lewis Acid Catalyzed One-Pot Selective Synthesis of Aminobenzofurans and N-Alkyl-2-aryl-2-(arylimino)acetamides: Product Dependence on the Nature of the Aniline |
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| Creator |
Mitra, Sudipta
Hota, Sandip K Chattopadhyay, Partha |
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| Subject |
Chemistry
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| Description |
An efficient one-pot reaction between isocyanides, anilines, and salicylaldehydes (2-hydroxybenzaldehydes) in the presence of a Lewis acid proceeds smoothly at room temperature within a short time interval to afford aminobenzofurans and Nalkyl- 2-aryl-2-(arylimino)acetamide derivatives in high yields depending on the electron density of the aniline component. |
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| Date |
2010
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| Type |
Article
PeerReviewed |
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| Format |
application/pdf
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| Identifier |
http://www.eprints.iicb.res.in/16/1/SYNTHESIS%2DSTUTTGART(22)3899%2D3905;2010[22].pdf
Mitra, Sudipta and Hota, Sandip K and Chattopadhyay, Partha (2010) Lewis Acid Catalyzed One-Pot Selective Synthesis of Aminobenzofurans and N-Alkyl-2-aryl-2-(arylimino)acetamides: Product Dependence on the Nature of the Aniline. Synthesis, 22. pp. 3899-3905. |
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| Relation |
http://dx.doi.org/10.1055/s-0030-1258239
http://www.eprints.iicb.res.in/16/ |
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