Nonlinear chiral interactions in resolutions with benzylamine derivatives

Emese Pálovics, E. Fogassy, J. Schindler, Mihály Nógrádi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

N-formylphenylalanine was subjected to optical resolution using a chiral agent such as phenylethylamine enantiomer, (R)-phenylglycine methyl ester, (S)-N-benzyl-2-aminobutanol, alone or in a mixture with each other or in a mixture with benzylamine.

Original languageEnglish
Pages (from-to)1-4
Number of pages4
JournalChirality
Volume19
Issue number1
DOIs
Publication statusPublished - 2006

Fingerprint

Phenethylamines
Derivatives
Enantiomers
Esters
benzylamine
methyl phenylglycine

Keywords

  • Enantiomer mixtures
  • Nonlinear effects
  • Optical resolution
  • Relations of structures

ASJC Scopus subject areas

  • Analytical Chemistry
  • Drug Discovery
  • Organic Chemistry
  • Pharmacology

Cite this

Nonlinear chiral interactions in resolutions with benzylamine derivatives. / Pálovics, Emese; Fogassy, E.; Schindler, J.; Nógrádi, Mihály.

In: Chirality, Vol. 19, No. 1, 2006, p. 1-4.

Research output: Contribution to journalArticle

Pálovics, Emese ; Fogassy, E. ; Schindler, J. ; Nógrádi, Mihály. / Nonlinear chiral interactions in resolutions with benzylamine derivatives. In: Chirality. 2006 ; Vol. 19, No. 1. pp. 1-4.
@article{5de65c5faa0544c88a5b5df039aa8141,
title = "Nonlinear chiral interactions in resolutions with benzylamine derivatives",
abstract = "N-formylphenylalanine was subjected to optical resolution using a chiral agent such as phenylethylamine enantiomer, (R)-phenylglycine methyl ester, (S)-N-benzyl-2-aminobutanol, alone or in a mixture with each other or in a mixture with benzylamine.",
keywords = "Enantiomer mixtures, Nonlinear effects, Optical resolution, Relations of structures",
author = "Emese P{\'a}lovics and E. Fogassy and J. Schindler and Mih{\'a}ly N{\'o}gr{\'a}di",
year = "2006",
doi = "10.1002/chir.20330",
language = "English",
volume = "19",
pages = "1--4",
journal = "Chirality",
issn = "0899-0042",
publisher = "Wiley-Liss Inc.",
number = "1",

}

TY - JOUR

T1 - Nonlinear chiral interactions in resolutions with benzylamine derivatives

AU - Pálovics, Emese

AU - Fogassy, E.

AU - Schindler, J.

AU - Nógrádi, Mihály

PY - 2006

Y1 - 2006

N2 - N-formylphenylalanine was subjected to optical resolution using a chiral agent such as phenylethylamine enantiomer, (R)-phenylglycine methyl ester, (S)-N-benzyl-2-aminobutanol, alone or in a mixture with each other or in a mixture with benzylamine.

AB - N-formylphenylalanine was subjected to optical resolution using a chiral agent such as phenylethylamine enantiomer, (R)-phenylglycine methyl ester, (S)-N-benzyl-2-aminobutanol, alone or in a mixture with each other or in a mixture with benzylamine.

KW - Enantiomer mixtures

KW - Nonlinear effects

KW - Optical resolution

KW - Relations of structures

UR - http://www.scopus.com/inward/record.url?scp=33845588546&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33845588546&partnerID=8YFLogxK

U2 - 10.1002/chir.20330

DO - 10.1002/chir.20330

M3 - Article

C2 - 16977610

AN - SCOPUS:33845588546

VL - 19

SP - 1

EP - 4

JO - Chirality

JF - Chirality

SN - 0899-0042

IS - 1

ER -