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Trends in the Synthesis and Functionalization of Guaianolides

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URI: http://hdl.handle.net/10498/20321

DOI: 10.1002/ejoc.201403244

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2015-Trends in the synthesis and functionalization of guaianolides.pdf (5.391Mb)
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Author/s
Santana, Alejandro; González Molinillo, José MaríaAuthority UCA; Macías Domínguez, Francisco AntonioAuthority UCA
Date
2015-01
Department
Química Orgánica
Source
Eur. J. Org. Chem. 2015, 2093–2110
Abstract
Guaianolides constitute a large and diverse group of biologically active sesquiterpenes. Guaianolide and seco-guaianolides can also be used as, for example, scaffolds for the development of new active molecules that are readily accessible by synthetic methods. Nevertheless, these lactones often have complex structures that make their synthesis difficult. The aim of this microreview is to provide an overview of the developments in guaianolide synthesis by the two major synthetic strategies: semi-synthesis and total synthesis. Partial and total syntheses of guaianolides are described, with particular emphasis placed on the methods reported in the last decade. The methods discussed include rearrangements, cycloadditions, ring-closing metathesis, the use of transitionmetal catalysts, photochemical reactions, and other recently developed techniques as key steps.
Subjects
total synthesis; natural products; terpenoids; lactones; guaianolides
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  • Artículos Científicos [4205]
  • Artículos Científicos INBIO [242]
  • Articulos Científicos Quim. Org. [158]
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
This work is under a Creative Commons License Attribution-NonCommercial-NoDerivatives 4.0 Internacional

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