Steroid Synthesis By High Pressure Diels-Alder Reaction Of 3-Methyl-2-Cyclopenten-1-One

E. Gács-Baitz, Assunta Marrocchi, Lucio Minuti, Hans W. Scheerens, Aldo Taticchi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A new regioselective and diastereoselective approach to the one-step synthesis of steroid skeleton based on high pressure Diels-Alder reaction of 3-methyl-2-cyclopenten-1-one is described. Structure analysis of the reaction products by NMR spectroscopy is presented.

Original languageEnglish
Pages (from-to)165-170
Number of pages6
JournalNatural Product Letters
Volume5
Issue number3
DOIs
Publication statusPublished - Nov 1 1994

Fingerprint

Cycloaddition Reaction
Reaction products
Skeleton
Nuclear magnetic resonance spectroscopy
steroids
skeleton
nuclear magnetic resonance spectroscopy
Magnetic Resonance Spectroscopy
Steroids
Pressure
synthesis
cyclopentenone
cycloaddition reactions

Keywords

  • 1-ethenylhydronaphthalene
  • 9-methyl-trans-Δ-octalone-l
  • Diels-Alder reaction
  • high pressure
  • NMR analysis
  • steroids

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Steroid Synthesis By High Pressure Diels-Alder Reaction Of 3-Methyl-2-Cyclopenten-1-One. / Gács-Baitz, E.; Marrocchi, Assunta; Minuti, Lucio; Scheerens, Hans W.; Taticchi, Aldo.

In: Natural Product Letters, Vol. 5, No. 3, 01.11.1994, p. 165-170.

Research output: Contribution to journalArticle

Gács-Baitz, E. ; Marrocchi, Assunta ; Minuti, Lucio ; Scheerens, Hans W. ; Taticchi, Aldo. / Steroid Synthesis By High Pressure Diels-Alder Reaction Of 3-Methyl-2-Cyclopenten-1-One. In: Natural Product Letters. 1994 ; Vol. 5, No. 3. pp. 165-170.
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