Sergio Emilio García Garrido

Dr. Sergio Emilio García Garrido

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Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 November 2007 in Chemical Society Reviews
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Philip GalePhilip Gale
Philip Gale
SGSergio Emilio García Garrido
Sergio Emilio García Garrido
JGJoachim Garric
Joachim Garric
This critical review covers advances in anion complexation chemistry related to receptors based on organic frameworks in the years 2005–2006. The review covers anion receptors that employ amides and thioamides, pyrroles and indoles, ureas and thioureas, ammonium, guanidinium, imidazolium, and receptors containing hydroxyl groups. There is a discussion of anion templated assembly, followed by a short section outlining modelling studies of these systems. (226 references.)

8 February 2010 in Dalton Transactions
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Victorio CadiernoVictorio Cadierno
Victorio Cadierno
PCPascale Crochet
Pascale Crochet
SGSergio Emilio García Garrido
Sergio Emilio García Garrido
JGJosé Gimeno
José Gimeno
The catalytic isomerization of propargylic alcohols promoted by transition-metals represents a straightforward and appealing route to synthetically useful α,β-unsaturated carbonyl compounds. Three different reaction pathways are known for these atom-economical transformations: (i) the so-called Meyer–Schuster and Rupe rearrangements, in which a formal 1,3- or 1,2-shift of the hydroxyl group takes place, and (ii) the redox-type isomerization, which involves a simultaneous oxidation of the alcohol unit and reduction of the CC bond. In this Perspective article an overview of the different metal catalysts presently available to promote these isomerization reactions, their mechanisms of action as well as relevant synthetic applications, is provided.

6 January 2006 in Journal of the American Chemical Society
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Victorio CadiernoVictorio Cadierno
Victorio Cadierno
SGSergio Emilio García Garrido
Sergio Emilio García Garrido
JGJosé Gimeno
José Gimeno
AVAdrián Varela-Álvarez
Adrián Varela-Álvarez
JSJosé A. Sordo
José A. Sordo

18 November 2010 in ChemSusChem
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SGSergio Emilio García Garrido
Sergio Emilio García Garrido
JFJavier Francos
Javier Francos
Victorio CadiernoVictorio Cadierno
Victorio Cadierno
JBJean-Marie Basset
Jean-Marie Basset
VPVivek Polshettiwar
Vivek Polshettiwar

1 November 2006 in Journal of the American Chemical Society
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Journal Article
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Victorio CadiernoVictorio Cadierno
Victorio Cadierno
SGSergio Emilio García Garrido
Sergio Emilio García Garrido
JGJosé Gimeno
José Gimeno

26 January 2007 in Chemical Communications
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SGSergio Emilio García Garrido
Sergio Emilio García Garrido
CCClaudia Caltagirone
Claudia Caltagirone
MLMark Light
Mark Light
Philip GalePhilip Gale
Philip Gale
The interaction of a variety of acridinone derivatives containing hydrogen-bond donor groups in the 4- and 5-positions with anions demonstrate the potential of this new scaffold in anion receptor and sensor design.