Synthesis of new conformationally rigid paramagnetic α-amino acids

Mária Balog, T. Kalai, J. Jekó́, Z. Berente, Heinz Jürgen Steinhoff, Martin Engelhard, K. Hideg

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

A pyrroline nitroxide based cyclic tetrasubstituted α-amino acid and paramagnetic homoproline and their derivatives are described. Introduction of a new paramagnetic protecting group to follow the incorporation of an amino acid into peptides by EPR is also suggested.

Original languageEnglish
Pages (from-to)145-149
Number of pages5
JournalTetrahedron Letters
Volume44
Issue number51
DOIs
Publication statusPublished - Dec 15 2003

Fingerprint

Cyclic Amino Acids
Paramagnetic resonance
Derivatives
Amino Acids
Peptides
homoproline
pyrroline

Keywords

  • Amino acids
  • Nitroxides
  • Protecting group
  • TOAC

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthesis of new conformationally rigid paramagnetic α-amino acids. / Balog, Mária; Kalai, T.; Jekó́, J.; Berente, Z.; Steinhoff, Heinz Jürgen; Engelhard, Martin; Hideg, K.

In: Tetrahedron Letters, Vol. 44, No. 51, 15.12.2003, p. 145-149.

Research output: Contribution to journalArticle

Balog, Mária ; Kalai, T. ; Jekó́, J. ; Berente, Z. ; Steinhoff, Heinz Jürgen ; Engelhard, Martin ; Hideg, K. / Synthesis of new conformationally rigid paramagnetic α-amino acids. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 51. pp. 145-149.
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