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      Total Synthesis of Transtaganolide E and F: Insight in the Biosynthesis of the Transtaganolides : Total Synthesis of Transtaganolide E and F

      , , , ,
      European Journal of Organic Chemistry
      Wiley-Blackwell

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          Progress toward the Synthesis of the Basiliolides and Transtaganolides:  An Intramolecular Pyrone Diels−Alder Entry into a Novel Class of Natural Products

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            A pyran-2-one and four meroterpenoids from Thapsia transtagana and their implication in the biosynthesis of transtaganolides.

            Four meroterpenoids (3a, 3b, 4 and 5), a prenylated pyran-2-one (2) along with the known compounds 7-O-geranylscopoletin (1), and thapsitranstagin (6) have been isolated from the roots of Thapsia transtagana. The presence of 1 and 2 supports the biogenetic hypothesis that transtaganolides, a group of bioactive metabolites, are meroterpenoids which come from an O-prenylated coumarin via successive pericyclic reactions.
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              Progress toward the synthesis of the transtaganolide/basiliolide natural products: an Ireland–Claisen approach

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                Author and article information

                Journal
                European Journal of Organic Chemistry
                Eur. J. Org. Chem.
                Wiley-Blackwell
                1434193X
                October 2013
                October 11 2013
                : 2013
                : 30
                : 6955-6960
                Article
                10.1002/ejoc.201301092
                aea3ed5d-649a-4bcc-a3c6-ac1c5007a5ce
                © 2013

                http://doi.wiley.com/10.1002/tdm_license_1.1

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