Molecular study on the enantiomeric relationships of carvedilol fragment A, 4-(2-hydroxypropoxy)carbazol, along with selected analogues

David R P Almeida, Donna M. Gasparro, Luca F. Pisterzi, Ladislaus L. Torday, A. Varró, J. Papp, B. Penke, I. Csizmadia

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The enantiomeric relationships of carvedilol fragment A, 4-(2-Hydroxypropoxy)carbazol, along with selected analogues were analyzed. The stereogenic units and optical isomerism describe the chiral disposition of electron density about nuclei. It was found that like enantiomers of point chirality, axis chiral conformers also occur in pairs.

Original languageEnglish
Pages (from-to)5594-5610
Number of pages17
JournalJournal of Physical Chemistry A
Volume107
Issue number29
DOIs
Publication statusPublished - Jul 21 2003

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Enantiomers
Chirality
enantiomers
chirality
Carrier concentration
fragments
analogs
nuclei
carvedilol

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

Molecular study on the enantiomeric relationships of carvedilol fragment A, 4-(2-hydroxypropoxy)carbazol, along with selected analogues. / Almeida, David R P; Gasparro, Donna M.; Pisterzi, Luca F.; Torday, Ladislaus L.; Varró, A.; Papp, J.; Penke, B.; Csizmadia, I.

In: Journal of Physical Chemistry A, Vol. 107, No. 29, 21.07.2003, p. 5594-5610.

Research output: Contribution to journalArticle

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