The synthesis of (±)-coronafacic acid by a tandem Wessely oxidation–Diels–Alder reaction sequence
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 10,p. 739-740
- https://doi.org/10.1039/c39900000739
Abstract
(±)-Coronafacic acid (9) has been synthesized from ethyl 5-(4-ethyl-2-hydroxyphenyl)pent-2-enoate (4)via a tandem Wessely oxidation–Diels–Alder reaction sequence.Keywords
This publication has 11 references indexed in Scilit:
- Tandem Wessely oxidation and intramolecular Diels–Alder reactions. III. Synthesis of isotwistanesCanadian Journal of Chemistry, 1988
- Total synthesis of d,l-coronafacic acid by an intermolecular Diels–Alder approachCanadian Journal of Chemistry, 1984
- A general synthesis of isotwist-8-en-2-ones from -(3-butenyl)phenolsTetrahedron Letters, 1983
- Intramolecular Lewis-acid promoted (2+2) cycloadditions: An efficient total synthesis of (±)-coronafacic acid via an internal Diels-Alder reaction.Tetrahedron Letters, 1981
- TOTAL SYNTHESIS OF (±)-CORONAFACIC ACIDChemistry Letters, 1981
- Palladium catalysis in natural product synthesisPublished by Walter de Gruyter GmbH ,1981
- Synthesis of (.+-.)-coronafacic acid. Efficient intramolecular Diels-Alder reaction of latent diene-dienophile functionality via thermal reactionJournal of the American Chemical Society, 1980
- Total synthesis of (.+-.)-coronafacic acid: use of anionic oxy-Cope rearrangements on aromatic substrates in synthesisJournal of the American Chemical Society, 1980
- Synthesis of (±)-coronafacic acidTetrahedron Letters, 1977
- Intramolekulare Diels‐Alder‐Additionen in 6‐(But‐3‐enyl)‐6‐methyl‐cyclohexa‐2,4‐dien‐1‐on‐Systemen; eine neue Synthese von TwistanderivatenHelvetica Chimica Acta, 1972