| Literature DB >> 12568608 |
Keiji Tanino1, Kei Onuki, Kohei Asano, Masaaki Miyashita, Tsuyoshi Nakamura, Yoshinori Takahashi, Isao Kuwajima.
Abstract
Total synthesis of ingenol, a diterpene isolated from the genus Euphorbia, was accomplished on the basis of the novel key reactions. The highly strained ingenane skeleton was constructed through an intramolecular cyclization reaction of an acetylene dicobalt complex followed by a rearrangement reaction of an epoxy alcohol. The C(3),C(4),C(5)-triol moiety was introduced by a stereoselective double dihydroxylation reaction of a diene having C(2)-C(3) and C(4)-C(5) double bonds.Entities:
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Year: 2003 PMID: 12568608 DOI: 10.1021/ja029226n
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419