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Eleuthesides and their analogs: XII. Alternative intramolecular ketalization with the formation of eunicellane tricyclic structure

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RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
卷 52, 期 7, 页码 978-982

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MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S1070428016070095

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  1. Russian Foundation for Basic Research [14-03-97007-r_povolzh'e_a]
  2. President's scholarship for young scientists [SP-1934.2015.4]

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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[9.3.1.0(3,8)]pentadeca-5,9,12-triene tricyclic system.

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