Homogeneous and heterogeneous catalytic asymmetric reactions IV. Hydrogenation of the Ni complexes of cinnamic acid salts over MRNi catalyst

M. Bartók, G. Wittmann, Gizella B. Bartók, György Göndös

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Substituted cinnamic acids containing a prochiral CC bond, and their LiI, KI, NiII and CaII salts, were prepared and their surface complexes on Ni were studied over a Raney-Ni catalyst modified with tartaric acid. The hydrogenation product of sodium cinnamate is optically active. Of the alkali metal salts of (E)-α-phenylcinnamic acid, the hydrogenation of the Na salt gives the highest optical yield (17%). The solvent used significantly influences the selectivity. The published data for the chiral RH complexes are listed for comparison with the results of the homogeneous and heterogeneous hydrogenations described. The enantioselectivity in the presence of Raney-Ni is the result of a complex formed by the interaction of (R,R)-tartaric acid with the substrate.

Original languageEnglish
Pages (from-to)385-395
Number of pages11
JournalJournal of Organometallic Chemistry
Volume384
Issue number3
DOIs
Publication statusPublished - Mar 6 1990

Fingerprint

Hydrogenation
hydrogenation
Salts
salts
catalysts
acids
Catalysts
Acids
Cinnamates
Alkali Metals
Enantioselectivity
Alkali metals
Sodium
alkali metals
selectivity
sodium
Substrates
cinnamic acid
products
tartaric acid

ASJC Scopus subject areas

  • Biochemistry
  • Chemical Engineering (miscellaneous)
  • Inorganic Chemistry
  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Materials Science (miscellaneous)
  • Materials Chemistry

Cite this

Homogeneous and heterogeneous catalytic asymmetric reactions IV. Hydrogenation of the Ni complexes of cinnamic acid salts over MRNi catalyst. / Bartók, M.; Wittmann, G.; Bartók, Gizella B.; Göndös, György.

In: Journal of Organometallic Chemistry, Vol. 384, No. 3, 06.03.1990, p. 385-395.

Research output: Contribution to journalArticle

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