Title of article :
4-Isocyanopermethylbutane-1,1,3-triol (IPB): a convertible isonitrile for multicomponent reactions
Author/Authors :
Neves Filho، نويسنده , , Ricardo A.W. and Stark، نويسنده , , Sebastian and Morejon، نويسنده , , Micjel C. and Westermann، نويسنده , , Bernhard and Wessjohann، نويسنده , , Ludger A.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2012
Pages :
4
From page :
5360
To page :
5363
Abstract :
The synthesis and applications of 4-isocyanopermethylbutane-1,1,3-triol (IPB) as a new convertible isonitrile (isocyanide) for isocyanide-based multicomponent reactions (IMCRs) like Ugi, Ugi-Smiles, and Passerini reactions are described. The primary products obtained from these IMCRs can be converted into highly activated N-acylpyrroles, which upon treatment with nucleophiles can be transformed into carboxylic acids, esters, amides, alcohols, and olefins. In this sense the reagent can be seen as a neutral carbanion equivalent to formate (HO2C−), and carboxylates or carboxamides etc. (RNu-CO−).
Keywords :
Activated amides , Activated carboxylic acids , Ugi reaction , Passerini reaction , Formate carbanion equivalent , Ugi-Smiles reaction , Functional group interconversions , N-Acylpyrroles , Isocyanides
Journal title :
Tetrahedron Letters
Serial Year :
2012
Journal title :
Tetrahedron Letters
Record number :
1882145
Link To Document :
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