Ramon Subirós‐Funosas

Centre for Inflammation Research — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index1.3kcitations30works0.02yr avg
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Research Topics

Chemical Synthesis and Analysis(21), Click Chemistry and Applications(15), Carbohydrate Chemistry and Synthesis(5), Chemical Synthesis and Reactions(4), Nanoplatforms for cancer theranostics(3)

Publications30 total

A Bivalent Activatable Fluorescent Probe for Screening and Intravital Imaging of Chemotherapy‐Induced Cancer Cell Death
Angewandte Chemie·2021· 7 citedOpen Access
A Bivalent Activatable Fluorescent Probe for Screening and Intravital Imaging of Chemotherapy‐Induced Cancer Cell Death
Angewandte Chemie International Edition·2021· 22 citedOpen Access
A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
Nature Communications·2020· 70 citedOpen Access
Fluorogenic Trp(redBODIPY) cyclopeptide targeting keratin 1 for imaging of aggressive carcinomas
Chemical Science·2019· 59 citedOpen Access
Fluorogenic peptides for the detection of programmed cell death
Proceedings of the 35th European Peptide Symposium·2018Open Access
A fluorescent activatable probe for imaging intracellular Mg<sup>2+</sup>
Organic & Biomolecular Chemistry·2017· 20 citedOpen Access
Chemical Modulation of <i>in Vivo</i> Macrophage Function with Subpopulation-Specific Fluorescent Prodrug Conjugates
ACS Central Science·2017· 80 citedOpen Access
Preparation of a Trp-BODIPY fluorogenic amino acid to label peptides for enhanced live-cell fluorescence imaging
Nature Protocols·2017· 66 citedOpen Access
A Trp-BODIPY cyclic peptide for fluorescence labelling of apoptotic bodies
Chemical Communications·2016· 76 citedOpen Access
ChemInform Abstract: Advances in Acylation Methodologies Enabled by Oxyma‐Based Reagents
ChemInform·2014· 16 cited
Low‐epimerization Peptide Bond Formation with Oxyma Pure: Preparation of<scp>Z</scp>‐<scp><i>L</i></scp>‐Phg‐Val‐OMe
Organic Syntheses·2014· 2 cited
Organophosphinic Coupling Reagents in Peptide Synthesis
2014
BOP‐OXy, BOP‐OBt, and BOP‐OAt: novel organophosphinic coupling reagents useful for solution and solid‐phase peptide synthesis
Journal of Peptide Science·2013· 8 cited
K‐Oxyma: a Strong Acylation‐Promoting, 2‐CTC Resin‐Friendly Coupling Additive
European Journal of Organic Chemistry·2013· 36 cited
COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents
Journal of Peptide Science·2013· 43 cited
Oxyma Pureを用いる低エピマー化ペプチド結合生成 Z-L-Phg-Val-OMeの調製
Organic Syntheses·2013
Screening of <i>N‐</i>Alkyl‐Cyanoacetamido Oximes as Substitutes for <i>N‐</i>Hydroxysuccinimide
ChemistryOpen·2012· 15 citedOpen Access
Ethyl 2-Cyano-2-(hydroxyimino)acetate
Encyclopedia of Reagents for Organic Synthesis·2012· 1 cited
Cyanoacetamide-based oxime carbonates: an efficient, simple alternative for the introduction of Fmoc with minimal dipeptide formation
Tetrahedron·2012· 11 cited
ChemInform Abstract: Aspartimide Formation in Peptide Chemistry: Occurrence, Prevention Strategies and the Role of N‐Hydroxylamines
ChemInform·2012
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Frequent Co-authors

Fernando Alberício(23), Ayman El‐Faham(16), Marc Vendrell(9), Nicole D. Barth(7), Lorena Mendive‐Tapia(7), Sherine N. Khattab(7), Ian Dransfield(5), Rodolfo Lavilla(4), Jesús Sot(3), Félix M. Goñi(3), Rodolfo Lavilla(3), Mikala Egeblad(3), Ouldouz Ghashghaei(3), Lidia Nieto‐Rodriguez(3), Rafel Prohens(2), Rodger Duffin(2), Adriano G. Rossi(2), Gerardo Acosta(2), Laura Maiorino(2), Xue‐Yan He(2)