电邮这篇文章 Eleuthesides and their analogs: XII. Alternative intramolecular ketalization with the formation of eunicellane tricyclic structure
- 作者: Sharipov B.T.1, Pershin A.A.1, Salikhov S.M.1, Valeev F.A.1
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隶属关系:
- Ufa Institute of Chemistry
- 期: 卷 52, 编号 7 (2016)
- 页面: 978-982
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/214673
- DOI: https://doi.org/10.1134/S1070428016070095
- ID: 214673
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详细
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.
作者简介
B. Sharipov
Ufa Institute of Chemistry
编辑信件的主要联系方式.
Email: sinvmet@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
A. Pershin
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
Sh. Salikhov
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
F. Valeev
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054 Bashkortostan
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