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Alejandro F. Barrero

Researcher at University of Granada

Publications -  317
Citations -  5875

Alejandro F. Barrero is an academic researcher from University of Granada. The author has contributed to research in topics: Radical cyclization & Catalysis. The author has an hindex of 38, co-authored 313 publications receiving 5474 citations. Previous affiliations of Alejandro F. Barrero include University of Copenhagen & Institut de Chimie des Substances Naturelles.

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Bioactive metabolites from a marine-derived strain of the fungus Emericella variecolor.

TL;DR: From a marine-derived strain of the fungus Emericella variecolor, varitriol (1), varioxirane (2), dihydroterrein (3), and varixanthone (4), besides the known mold metabolites ergosterol, terrein, shamixanth one, and tajIXanthone hydrate, were identified.
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Titanocene‐Catalyzed Cascade Cyclization of Epoxypolyprenes: Straightforward Synthesis of Terpenoids by Free‐Radical Chemistry

TL;DR: Both theoretical and experimental evidence suggests that this titanocene-catalyzed cascade cyclization of epoxypolyenes takes place in a nonconcerted fashion via discrete carbon-centered radicals, and its end step can easily be controlled to give exocyclic double bonds by simply excluding water from the medium.
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New sources and antifungal activity of sesquiterpene lactones.

TL;DR: Results suggest that a relatively low polarity is one of the molecular requirements for the antifungal activity of sesquiterpene lactones.
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Weakening C-O bonds: Ti(III), a new reagent for alcohol deoxygenation and carbonyl coupling olefination.

TL;DR: Investigations detailed herein demonstrate that the formation of either alkoxy- or hydroxy-Ti(III) complexes considerably decreases the energy of activation for C-O bond homolysis, and two new synthetic applications of Nugent's reagent in organic chemistry are described.
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Titanocene‐Mediated Radical Cyclization: An Emergent Method Towards the Synthesis of Natural Products

TL;DR: The reaction of the Cp2TiCl complex with oxiranes leads to homolytic opening of the heterocycle with high regioselectivity as mentioned in this paper, where the resulting β-titanoxyl radical can evolve in different ways, when the epoxide reacting with CpTiCl possesses suitable unsaturated moieties such as olefins, triple bonds, carbonyls or nitriles in its structure, leading to a cyclization process.