Email this article Eleuthesides and their analogs: XII. Alternative intramolecular ketalization with the formation of eunicellane tricyclic structure
- Authors: Sharipov B.T.1, Pershin A.A.1, Salikhov S.M.1, Valeev F.A.1
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Affiliations:
- Ufa Institute of Chemistry
- Issue: Vol 52, No 7 (2016)
- Pages: 978-982
- Section: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/214673
- DOI: https://doi.org/10.1134/S1070428016070095
- ID: 214673
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Abstract
Removal of the acetonide protection in the synthesis of 7,8-epimer of eleutheside is accompanied by intramolecular cyclization with the formation of 15-oxatricyclo[9.3.1.03,8]pentadeca-5,9,12-triene tricyclic system.
About the authors
B. T. Sharipov
Ufa Institute of Chemistry
Author for correspondence.
Email: sinvmet@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
A. A. Pershin
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
Sh. M. Salikhov
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
F. A. Valeev
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Russian Federation, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
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