A possible way for the introduction of α- and β-formyl-ethyl-substituents into the steroid-skeleton via coupling and carbonylation reactions

R. Skoda-Földes, L. Kollár, Bálint Heil, György Gálik, Zoltán Tuba, Antonio Arcade

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Cholesta-3,5-dien-3-yl triflate and androsta-16-en-17-yl iodide were vinylated with palladium and the olefins hydroformylated in the presence of rhodium and platinum catalysts.

Original languageEnglish
Pages (from-to)633-634
Number of pages2
JournalTetrahedron Asymmetry
Volume2
Issue number7
DOIs
Publication statusPublished - 1991

Fingerprint

Carbonylation
Rhodium
steroids
Palladium
Alkenes
Iodides
Platinum
rhodium
musculoskeletal system
Skeleton
iodides
alkenes
Olefins
palladium
platinum
Steroids
catalysts
Catalysts

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Organic Chemistry
  • Materials Chemistry
  • Drug Discovery

Cite this

A possible way for the introduction of α- and β-formyl-ethyl-substituents into the steroid-skeleton via coupling and carbonylation reactions. / Skoda-Földes, R.; Kollár, L.; Heil, Bálint; Gálik, György; Tuba, Zoltán; Arcade, Antonio.

In: Tetrahedron Asymmetry, Vol. 2, No. 7, 1991, p. 633-634.

Research output: Contribution to journalArticle

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AU - Tuba, Zoltán

AU - Arcade, Antonio

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