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Synlett 1997; 1997(SI): 493-494
DOI: 10.1055/s-1997-6116
DOI: 10.1055/s-1997-6116
letter
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Total Synthesis of Endiandric Acid A via an Intramolecular Diels-Alder Strategy
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
![](https://www.thieme-connect.de/media/synlett/1997SupI/lookinside/thumbnails/10.1055-s-1997-6116-1.jpg)
The total synthesis of endiandric acid A (1), featuring an intramolecular Diels-Alder approach for elaboration of the 6-5-6 carbocyclic array and an intramolecular Majetich reaction for construction of the four-membered ring, is described.
endiandric acid A - Majetich cyclobutane annulation - intramolecular Diels-Alder - 5.0 lithium perchlorate-diethyl ether - trimethylsilyl triflate