The preparation of methyl 9-iodo-perfluorononanoate: An access to reverse fluorinated amphiphiles

Zoltán Szlávik, A. Csámpai, Marie Pierre Krafft, Jean G. Riess, J. Rábai

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

ω-Functionalized F-alkyl iodides are useful building blocks of compounds containing perfluroalkyl segments in an inner position. A convenient and effective synthesis of methyl 9-iodoperfluorononanoate, a precursor molecule of this kind, is described, as well as the synthesis of a member of a new class of amphiphiles, revere F-amphiphiles.

Original languageEnglish
Pages (from-to)8757-8760
Number of pages4
JournalTetrahedron Letters
Volume38
Issue number50
Publication statusPublished - Dec 15 1997

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Amphiphiles
Iodides
Molecules
hexadecafluoro-nonanoic acid

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

The preparation of methyl 9-iodo-perfluorononanoate : An access to reverse fluorinated amphiphiles. / Szlávik, Zoltán; Csámpai, A.; Krafft, Marie Pierre; Riess, Jean G.; Rábai, J.

In: Tetrahedron Letters, Vol. 38, No. 50, 15.12.1997, p. 8757-8760.

Research output: Contribution to journalArticle

Szlávik, Zoltán ; Csámpai, A. ; Krafft, Marie Pierre ; Riess, Jean G. ; Rábai, J. / The preparation of methyl 9-iodo-perfluorononanoate : An access to reverse fluorinated amphiphiles. In: Tetrahedron Letters. 1997 ; Vol. 38, No. 50. pp. 8757-8760.
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