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Juan M. Cuerva

Researcher at University of Granada

Publications -  217
Citations -  5030

Juan M. Cuerva is an academic researcher from University of Granada. The author has contributed to research in topics: Catalysis & Allylic rearrangement. The author has an hindex of 39, co-authored 201 publications receiving 4071 citations. Previous affiliations of Juan M. Cuerva include Autonomous University of Madrid.

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Water: The Ideal Hydrogen‐Atom Source in Free‐Radical Chemistry Mediated by TiIII and Other Single‐Electron‐Transfer Metals?

TL;DR: Solid evidence is shown to show that water really can act as a complete hydrogen-atom source rather than as a simple proton donor for radical reductions mediated by Ti and, presumably, other metals that react by single-electron transfer.
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Undecabenzo[7]superhelicene: A Helical Nanographene Ribbon as a Circularly Polarized Luminescence Emitter

TL;DR: The synthesis and characterization of an enantiopure superhelicene nanographene is reported in which two saddle-shaped and one planar hexabenzocoronene (HBC) units are arranged in a helicoidal shape to form an undecabenzo[7]carbohelicenes, the first fully π-extended [7] helicene.
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7-endo radical cyclizations catalyzed by titanocene(III). Straightforward synthesis of terpenoids with seven-membered carbocycles.

TL;DR: Theoretical and experimental evidence is provided in support of a plausible mechanism, which may rationalize the preference for the unusual 7-endo cyclization mode shown by radicals with substitution patterns characteristic of the linalyl, nerolidyl, and geranyl linalsyl systems.
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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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Understanding the Exceptional Hydrogen-Atom Donor Characteristics of Water in TiIII-Mediated Free-Radical Chemistry

TL;DR: This work demonstrates that the efficiency of titanocene(III) aqua complexes as an unique class of HAT reagents is based on two key features: excellent binding capabilities of water toward titanocene (III) complexes and a low activation energy for the HAT step.