The first enantioselective synthesis of α-aminophosphinates

Andrea Szabó, Zsuzsa M. Jászay, L. Hegedûs, L. Tőke, Imre Petneházy

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

The first enantioselective synthesis of substituted α-aminophosphinic acids was carried out by the addition of ethyl phenylphosphinate to chiral imines in the absence of base or other catalyst.

Original languageEnglish
Pages (from-to)4603-4606
Number of pages4
JournalTetrahedron Letters
Volume44
Issue number24
DOIs
Publication statusPublished - Jun 9 2003

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Imines
Catalysts
Acids

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

The first enantioselective synthesis of α-aminophosphinates. / Szabó, Andrea; Jászay, Zsuzsa M.; Hegedûs, L.; Tőke, L.; Petneházy, Imre.

In: Tetrahedron Letters, Vol. 44, No. 24, 09.06.2003, p. 4603-4606.

Research output: Contribution to journalArticle

Szabó, Andrea ; Jászay, Zsuzsa M. ; Hegedûs, L. ; Tőke, L. ; Petneházy, Imre. / The first enantioselective synthesis of α-aminophosphinates. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 24. pp. 4603-4606.
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