Literature DB >> 11911200

Seven-membered vibsane-type diterpenes with a 5,10-cis relationship from Viburnum awabuki.

Yoshiyasu Fukuyama1, Hiroyuki Minami, Asami Matsuo, Kanako Kitamura, Mie Akizuki, Miwa Kubo, Mitsuaki Kodama.   

Abstract

New five seven-membered vibsane-type diterpenes named 5-epi-vibsanin C, 5-epi-vibsanin H, 5-epi-vibsanin K, 18-O-methyl-5-epi-vibsanin K and 5-epi-vibsanin E have been isolated from the leaves of Viburnum awabuki (Caplifoliaceae). Their structures have been elucidated by analyses of spectroscopic data and comparison of their spectral data with those of the previously known seven-membered vibsane-type diterpenes. The occurrence of these seven-membered vibsane-type diterpenes with a cis relationship on the C-5 and C-10 positions in nature have been predicted by conformational analysis of vibsanin B, an eleven-membered vibsane-type diterpene. Vibsanin C, 5-epi-vibsanin C and 5-epi-vibsanin H exhibited moderate cytotoxic activities on KB cells.

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Year:  2002        PMID: 11911200     DOI: 10.1248/cpb.50.368

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  3 in total

1.  Asymmetric [4 + 3] cycloadditions between vinylcarbenoids and dienes: application to the total synthesis of the natural product (-)-5-epi-vibsanin E.

Authors:  Brett D Schwartz; Justin R Denton; Yajing Lian; Huw M L Davies; Craig M Williams
Journal:  J Am Chem Soc       Date:  2009-06-17       Impact factor: 15.419

Review 2.  Recent applications of the divinylcyclopropane-cycloheptadiene rearrangement in organic synthesis.

Authors:  Sebastian Krüger; Tanja Gaich
Journal:  Beilstein J Org Chem       Date:  2014-01-16       Impact factor: 2.883

3.  Cytotoxic and radical scavenging nor-dammarane triterpenoids from Viburnum mongolicum.

Authors:  Xiaohua Wang; Wei Wang
Journal:  Molecules       Date:  2013-01-24       Impact factor: 4.411

  3 in total

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