ChemInform Abstract: STEREOCONTROLLED INTRAMOLECULAR DIELS-ALDER REACTION OF HETERODIENES; STUDIES ON THE SYNTHESIS OF CANNABINOIDS

Lutz F. Tietze; G. VON KIEDROWSKI; Klaus Harms; W. Clegg; In Memory: G.M. Sheldrick (1942–2025)

doi:10.1002/chin.198021216

ChemInform Abstract: STEREOCONTROLLED INTRAMOLECULAR DIELS-ALDER REACTION OF HETERODIENES; STUDIES ON THE SYNTHESIS OF CANNABINOIDS

Chemischer Informationsdienst 11(21)

Article 1980 German

Abstract

1 min read

Die Umsetzung von (R)‐Citronellal (I) mit dem Enolat des Cyclohexandions (II) verläuft über eine 100proz. stereokontrollierte intramolekulare Diels‐Alder‐Reaktion eines intermediär gebildeten ogß‐ungesättigten Ketons zu dem tricyclischen Dihydropyran‐Derivat (III).

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ChemInform Abstract: STEREOCONTROLLED INTRAMOLECULAR DIELS-ALDER REACTION OF HETERODIENES; STUDIES ON THE SYNTHESIS OF CANNABINOIDS

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