Synthesis of perfluoroalkylated beta-alanine and some peptide derivatives: an access to original surfactants.

Amino Acids

Laboratoire de Chimie Physique Organique et Colloïdale, Université Henri Poincaré, Faculté des Sciences, Nancy-Vandoeuvre, France.

Published: August 1999

The reaction of amines of sodium azide with 3-perfluoroalkyl-3-fluoroprop-2-enoate, followed by hydrogenation, affords perfluoroalkylated beta-alanine analogues in very good yields. These compounds can be linked via an amide bond to produce peptide analogues such as carnosine or carcinine derivatives, which could have surfactive and complexing properties.

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http://dx.doi.org/10.1007/BF01388177DOI Listing

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Synthesis of perfluoroalkylated beta-alanine and some peptide derivatives: an access to original surfactants.

Amino Acids

August 1999

Laboratoire de Chimie Physique Organique et Colloïdale, Université Henri Poincaré, Faculté des Sciences, Nancy-Vandoeuvre, France.

The reaction of amines of sodium azide with 3-perfluoroalkyl-3-fluoroprop-2-enoate, followed by hydrogenation, affords perfluoroalkylated beta-alanine analogues in very good yields. These compounds can be linked via an amide bond to produce peptide analogues such as carnosine or carcinine derivatives, which could have surfactive and complexing properties.

View Article and Find Full Text PDF

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