QUÍMICA ORGÁNICA
DEPARTAMENTO
![Foto de Ruben](/img/nophoto.png)
Ruben
Tapia Martin
Publicaciones en las que colabora con Ruben Tapia Martin (14)
2021
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Octagon-Embedded Carbohelicene as a Chiral Motif for Circularly Polarized Luminescence Emission of Saddle-Helix Nanographenes
Angewandte Chemie - International Edition, Vol. 60, Núm. 11, pp. 6094-6100
2020
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Lipid analogs reveal features critical for hemolysis and diminish granadaene mediated Group B Streptococcus infection
Nature Communications, Vol. 11, Núm. 1
2019
2018
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Aggregation-induced emission of [3]cumulenes functionalized with heptagon-containing polyphenylenes
Chemical Communications, Vol. 54, Núm. 27, pp. 3359-3362
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Quantification of oleacein and oleuropein aglycone in olive oil using deuterated surrogates by normal-phase ultra high performance liquid chromatography with quadrupole time-of-flight mass spectrometry
Journal of Separation Science, Vol. 41, Núm. 23, pp. 4272-4280
2017
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Antiproliferative Activity of Natural Taiwaniaquinoids and Related Compounds
Journal of Natural Products, Vol. 80, Núm. 2, pp. 308-318
2014
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Stereoselective transformations of (+)-abietic acid into (+)-vitedoin B and (+)-negundoin A
Journal of Organic Chemistry, Vol. 79, Núm. 10, pp. 4405-4413
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The first synthesis of (-)-isoambreinolide, (+)-vitexifolin D and (+)-vitedoin B
Organic and Biomolecular Chemistry, Vol. 12, Núm. 4, pp. 667-672
2013
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I2-pph3 mediated spiroannulation of unsaturated β-dicarbonyl compounds. The first synthesis of (±)-negundoin a
Chemical Communications, Vol. 49, Núm. 87, pp. 10257-10259
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NIS-PPh3: A selective reagent for the spiroannulation of o-allyl phenols. total synthesis of corallidictyal D
Journal of Organic Chemistry, Vol. 78, Núm. 18, pp. 9196-9204
2012
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Estrategia general hacia taiwaniaquinoides bioactivos y primera metodología de síntesis de espiro enol éteres terpénicos naturales
Estrategia general hacia taiwaniaquinoides bioactivos y primera metodología de síntesis de espiro enol éteres terpénicos naturales
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General access to taiwaniaquinoids based on a hypothetical abietane C7-C8 cleavage biogenetic pathway
Journal of Organic Chemistry, Vol. 77, Núm. 1, pp. 573-584
2010
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Enantioselective total synthesis of cytotoxic taiwaniaquinones A and F
Chemical Communications, Vol. 46, Núm. 48, pp. 9244-9246
2009
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A convenient enantiospecific route towards bioactive merosesquiterpenes by cationic-resin-promoted Friedel-Crafts alkylation with α,β-enones
European Journal of Organic Chemistry, pp. 1139-1143