Literature DB >> 19806633

Photochemical key steps in the synthesis of surfactants from furfural-derived intermediates.

Abdoulaye Gassama1, Cédric Ernenwein, Norbert Hoffmann.   

Abstract

Furfural is oxidized to 2[5H]-furanone by using hydrogen peroxide or to 5-hydroxy-2[5H]-furanone by using photo-oxygenation. An amine function is introduced by photochemically induced radical addition of tertiairy amines, some of which carry an n-alkyl side chain as hydrophobic moiety. These amines are produced from fatty aldehydes and cyclic secondary amines. The resulting adducts are transformed into amphoteric surfactants possessing an ammonium and a carboxylate function. Amphoteric (pK(N) and isoelectric point) and surfactant properties such as the critical micelle concentration and the adsorption efficiency are determined.

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Year:  2009        PMID: 19806633     DOI: 10.1002/cssc.200900150

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  3 in total

Review 1.  5-Hydroxymethylfurfural and Furfural Chemistry Toward Biobased Surfactants.

Authors:  Xiaoyang Yue; Yves Queneau
Journal:  ChemSusChem       Date:  2022-02-09       Impact factor: 9.140

2.  Visible-light-induced, Ir-catalyzed reactions of N-methyl-N-((trimethylsilyl)methyl)aniline with cyclic α,β-unsaturated carbonyl compounds.

Authors:  Dominik Lenhart; Thorsten Bach
Journal:  Beilstein J Org Chem       Date:  2014-04-17       Impact factor: 2.883

3.  Synthesis and Antimalarial Activity of 1,4-Disubstituted Piperidine Derivatives.

Authors:  Rokhyatou Seck; Abdoulaye Gassama; Sandrine Cojean; Christian Cavé
Journal:  Molecules       Date:  2020-01-11       Impact factor: 4.411

  3 in total

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