Publications by the researcher in collaboration with Ruben Tapia Martin (14)

2021

  1. 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

  1. Lipid analogs reveal features critical for hemolysis and diminish granadaene mediated Group B Streptococcus infection

    Nature Communications, Vol. 11, Núm. 1

2019

  1. Direct determination of phenolic secoiridoids in olive oil by ultra-high performance liquid chromatography-triple quadruple mass spectrometry analysis

    Scientific Reports, Vol. 9, Núm. 1

2018

  1. Aggregation-induced emission of [3]cumulenes functionalized with heptagon-containing polyphenylenes

    Chemical Communications, Vol. 54, Núm. 27, pp. 3359-3362

  2. 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

  1. Antiproliferative Activity of Natural Taiwaniaquinoids and Related Compounds

    Journal of Natural Products, Vol. 80, Núm. 2, pp. 308-318

2014

  1. Stereoselective transformations of (+)-abietic acid into (+)-vitedoin B and (+)-negundoin A

    Journal of Organic Chemistry, Vol. 79, Núm. 10, pp. 4405-4413

  2. The first synthesis of (-)-isoambreinolide, (+)-vitexifolin D and (+)-vitedoin B

    Organic and Biomolecular Chemistry, Vol. 12, Núm. 4, pp. 667-672

2013

  1. I2-pph3 mediated spiroannulation of unsaturated β-dicarbonyl compounds. The first synthesis of (±)-negundoin a

    Chemical Communications, Vol. 49, Núm. 87, pp. 10257-10259

  2. 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

  1. 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

  2. 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

  1. Enantioselective total synthesis of cytotoxic taiwaniaquinones A and F

    Chemical Communications, Vol. 46, Núm. 48, pp. 9244-9246

2009

  1. 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