Comparison of chiral modifiers in the Pd catalysed hydrogenation of phenylcinnamic acid and isophorone

A. Tungler, Yuriko Nitta, Karina Fodor, Gabriella Farkas, Tibor Máthé

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

The asymmetric induction of (-)-dihydroapovincarninic acid ethyl ester [(-)-DHVIN] and cinchonidine employed as chiral modifiers was compared in the Pd catalysed hydrogenation of the C=C double bonds of phenylcinnamic acid and isophorone. The differences in their effect and behaviour were attributed to the difference in the interaction between the modifier and the reactant and to their different basicity.

Original languageEnglish
Pages (from-to)135-140
Number of pages6
JournalJournal of Molecular Catalysis A: Chemical
Volume149
Issue number1-2
DOIs
Publication statusPublished - Dec 15 1999

Fingerprint

Hydrogenation
hydrogenation
acids
Acids
Alkalinity
esters
Esters
induction
interactions
isophorone
cinchonidine

Keywords

  • Chiral modifier
  • Dihydroapovincaminic acid ethyl ester
  • Enantioselectivity
  • Hydrogenation
  • Isophorone
  • Phenylcinnamic acid

ASJC Scopus subject areas

  • Catalysis
  • Process Chemistry and Technology

Cite this

Comparison of chiral modifiers in the Pd catalysed hydrogenation of phenylcinnamic acid and isophorone. / Tungler, A.; Nitta, Yuriko; Fodor, Karina; Farkas, Gabriella; Máthé, Tibor.

In: Journal of Molecular Catalysis A: Chemical, Vol. 149, No. 1-2, 15.12.1999, p. 135-140.

Research output: Contribution to journalArticle

Tungler, A. ; Nitta, Yuriko ; Fodor, Karina ; Farkas, Gabriella ; Máthé, Tibor. / Comparison of chiral modifiers in the Pd catalysed hydrogenation of phenylcinnamic acid and isophorone. In: Journal of Molecular Catalysis A: Chemical. 1999 ; Vol. 149, No. 1-2. pp. 135-140.
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