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Wiley, European Journal of Organic Chemistry, 15(2014), p. 3097-3100, 2014

DOI: 10.1002/ejoc.201402170

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A three-step synthesis of the guaianolide ring system

Journal article published in 2014 by Jan Hullaert ORCID, Duchan R. Laplace, Johan M. Winne
This paper is available in a repository.
This paper is available in a repository.

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Abstract

By using a gallium(III) triflate catalyzed intramolecular (4+3) cycloaddition, a few functionalized furan-derived tricycles that share the common guaianolide sesquiterpene ring system were prepared in a stereoselective manner in only three steps from commercially available starting materials. A discussion of the formation of alternative products is included, with possible substrate requirements to achieve the key cycloaddition step in an efficient way.