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Publications

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Publications

[1]
G. Proietti et al., "Ultralight aerogels via supramolecular polymerization of a new chiral perfluoropyridine-based sulfonimidamide organogelator," Nanoscale, vol. 16, no. 15, pp. 7603-7611, 2024.
[2]
J. Huang et al., "Correlation between Polymerization Rate, Mechanism, and Conformer Thermodynamic Stability in Urea/Methoxide-Catalyzed Polymerization of Macrocyclic Carbonates," Macromolecules, vol. 56, no. 18, pp. 7496-7504, 2023.
[3]
C. Zhou et al., "Highly congested spiro-compounds via photoredox-mediated dearomative annulation cascade," Communications Chemistry, vol. 5, no. 1, 2022.
[4]
G. Proietti et al., "Nickel Boride Catalyzed Reductions of Nitro Compounds and Azides : Nanocellulose-supported Catalysts in Tandem Reactions," Synthesis (Stuttgart), vol. 54, no. 01, pp. 133-146, 2022.
[5]
G. Proietti et al., "Accessing Perfluoroaryl Sulfonimidamides and Sulfoximines via Photogenerated Perfluoroaryl Nitrenes : Synthesis and Application as a Chiral Auxiliary," Journal of Organic Chemistry, vol. 86, no. 23, pp. 17119-17128, 2021.
[6]
A. Shatskiy et al., "Back cover," Chemical Science, vol. 12, no. 15, pp. 5430-5437, 2021.
[7]
J. C. Zirignon et al., "Experimental review of PEI electrodeposition onto copper substrates for insulation of complex geometries," RSC Advances, vol. 11, no. 55, pp. 34599-34604, 2021.
[8]
A. Shatskiy et al., "Stereoselective synthesis of unnatural α-amino acid derivatives through photoredox catalysis," Chemical Science, vol. 12, no. 15, pp. 5430-5437, 2021.
[9]
J. Izquierdo et al., "Asymmetric Synthesis of Adjacent Tri- and Tetrasubstituted Carbon Stereocenters : Organocatalytic Aldol Reaction of an Hydantoin Surrogate with Azaarene 2-Carbaldehydes," Chemistry - A European Journal, 2019.
[10]
P. Wu, P. Dinér and L. Bunch, "CHAPTER 3 : The Screening and Design of Allosteric Kinase Inhibitors," in Kinase drug discovery : Modern approaches, : Royal Society of Chemistry, 2019, pp. 34-60.
[11]
B. Blomkvist and P. Dinér, "Mild and Rapid Aniline/HBF4 center dot DEE-Catalysed Formation of Sulfinyl Imines," ChemistrySelect, vol. 4, no. 25, pp. 7431-7436, 2019.
[12]
P. Josephson et al., "Student-Driven Development of Greener Chemistry in Undergraduate Teaching: Synthesis of Lidocaine Revisited," Journal of Chemical Education, 2019.
[13]
B. Blomkvist and P. Dinér, "HBF4 center dot DEE-catalyzed formation of sulfinyl imines : Synthesis and mechanistic studies," Tetrahedron Letters, vol. 59, no. 13, pp. 1249-1253, 2018.
[14]
B. Timmer et al., "Simple and Effective Integration of Green Chemistry and Sustainability Education into an Existing Organic Chemistry Course," Journal of Chemical Education, vol. 95, no. 8, pp. 1301-1306, 2018.
[15]
K. J. Prathap et al., "Catalytic Reductions and Tandem Reactions of Nitro Compounds Using in Situ Prepared Nickel Boride Catalyst in Nanocellulose Solution," Organic Letters, vol. 19, no. 18, pp. 4746-4749, 2017.
[16]
L. Wang et al., "A Nickel (II) PY5 Complex as an Electrocatalyst for Water Oxidation," Journal of Catalysis, vol. 335, pp. 72-78, 2016.
[17]
R. Hertzberg, P. Dinér and C. Moberg, "Palladium-Catalyzed C(sp3)–C(sp2) Cross-Couplings of O-(α-Bromoacyl) Cyanohydrins with Boronic Acids : An Entry to Enantio­enriched N-Acylated β-Amino Alcohols," Synthesis (Stuttgart), vol. 48, no. 19, 2016.
[18]
P. Dinér, "Yttrium from Ytterby," Nature Chemistry, vol. 8, no. 2, pp. 192-192, 2016.
[19]
L. Mesas-Sánchez and P. Dinér, "A Mechanistic Investigation of the Kinetic Resolution of Secondary Aromatic Alcohols Using a Ferrocene-Based Planar Chiral 4-(Dimethylamino)pyridine Catalyst," Chemistry - A European Journal, vol. 21, no. 14, pp. 5623-5631, 2015.
[20]
C. Hamngren Blomqvist et al., "A Single-Cell Study of a Highly Effective Hog1 Inhibitor for in Situ Yeast Cell Manipulation," Micromachines, vol. 5, no. 1, pp. 81-96, 2014.
[21]
A. E. Diaz-Alvarez, L. Mesas-Sanchez and P. Dinér, "Access to Optically Pure beta-Hydroxy Esters via Non-Enzymatic Kinetic Resolution by a Planar-Chiral DMAP Catalyst," Molecules, vol. 19, no. 9, pp. 14273-14291, 2014.
[22]
P. Dinér, A. Sadhukhan and B. Blomkvist, "Chiral Sulfinamides as Highly Enantioselective Organocatalysts," ChemCatChem, vol. 6, no. 11, pp. 3063-3066, 2014.
[23]
L. Mesas-Sanchez et al., "Kinetic resolution of 2-hydroxy-2-aryl-ethylphosphonates by a non-enzymatic acylation catalyst," Tetrahedron, vol. 70, no. 24, pp. 3807-3811, 2014.
[24]
J. P. Alao et al., "Selective inhibition of RET mediated cell proliferation in vitro by the kinase inhibitor SPP86," BMC Cancer, vol. 14, no. 853, 2014.
[25]
J.-F. Poon et al., "Azastilbenes : a cut-off to p38 MAPK inhibitors," Organic and biomolecular chemistry, vol. 11, no. 27, 2013.
[26]
J. J. Verendel and P. Dinér, "Efficient, Low Temperature Production of Hydrogen from Methanol," ChemCatChem, vol. 5, no. 10, pp. 2795-2797, 2013.
[27]
R. Amorati et al., "Multi-faceted reactivity of alkyltellurophenols towards peroxyl radicals : Catalytic antioxidant versus thiol-depletion effect," Chemistry - A European Journal, vol. 19, no. 23, pp. 7510-7522, 2013.
[28]
A. E. Díaz-Álvarez, L. Mesas-Sánchez and P. Dinér, "Nichtenzymatische dynamische kinetische Racematspaltung sekundärer Arylalkohole : planar-chirale Ferrocen- und Rutheniumkatalysatoren im Zusammenspiel," Angewandte Chemie International Edition, vol. 125, no. 2, pp. 522-524, 2013.
[29]
A. E. Díaz-Álvarez, L. Mesas Sanchez and P. Dinér, "Non-Enzymatic Dynamic Kinetic Resolution of Secondary Aryl Alcohols : Planar Chiral Ferrocene and Ruthenium Catalysts in Cooperation," Angewandte Chemie International Edition, vol. 52502-504, no. 2, pp. 502-504, 2013.
[30]
L. Mesas-Sánchez, A. E. Díaz-Álvarez and P. Dinér, "Non-enzymatic kinetic resolution of 1,2-azidoalcohols using a planar-chiral DMAP derivative catalyst," Tetrahedron, vol. 69, no. 2, pp. 753-757, 2013.
[31]
C. Hamngren Blomqvist et al., "Design and evaluation of a microfluidic system for inhibition studies of yeast cell signaling," in Proceedings of SPIE : Optical Trapping and Optical Micromanipulation IX, 2012, p. 84582K.
[32]
P. Dinér et al., "Preparation of 3-Substituted-1-Isopropyl-1H-pyrazolo 3,4-d pyrimidin-4-amines as RET Kinase Inhibitors," Journal of Medicinal Chemistry, vol. 55 4872-4876, no. 10, pp. 4872-4876, 2012.
[33]
P. Dinér, "Superacid-Promoted Ionization of Alkanes Without Carbonium Ion Formation : A Density Functional Theory Study," Journal of Physical Chemistry A, vol. 116, no. 40, pp. 9979-9984, 2012.
[34]
A. Dierckx et al., "Characterization of photophysical and base-mimicking properties of a novel fluorescent adenine analogue in DNA," Nucleic Acids Research, vol. 34, no. 10, pp. 4513-4524, 2011.
[35]
C. Dyrager et al., "Design, synthesis, and biological evaluation of chromone-based p38 MAP kinase inhibitors," Journal of Medicinal Chemistry, vol. 54, 2011.
[36]
P. Dinér et al., "Design, synthesis, and characterization of a highly effective Hog1 inhibitor : a powerful tool for analyzing MAP kinase signaling in yeast," PLOS ONE, vol. 6, no. 5, 2011.
[37]
P. Dinér, "Catalytic asymmetric chiral lithium amide-promoted epoxide rearrangement : a NMR spectroscopic and kinetic investigation," Tetrahedron : asymmetry, vol. 21, no. 21-22, pp. 2733-2739, 2010.
[38]
P. Dinér et al., "Design, synthesis and characterization of a highly effective Hog1 inhibitor : a powerful tool for analyzing MAP kinase signaling in yeast," in Special Issue: Abstracts of the 35th FEBS Congress, Gothenburg, Sweden, 26 June - 1 July 2010, 2010.
[39]
P. Dinér et al., "Design, synthesis and characterization of a highly effective Hog1 inhibitor : a powerful tool for analyzing MAP kinase signalling in yeast," in Yeast Genetics and Molecular Biology Meeting, Vancouver, Canada, 2010.
[40]
P. Dinér et al., "Highly selective, cell-permeable and fast-acting wild-type Hog1 inhibitors as tools for studying cellular function of kinases," in Functional Genomics Symposium: Chemical Biology – Molecules to Probe Life, Gothenburg, Sweden, 2009.
[41]
P. Dinér et al., "Short cut to 1,2,3-triazole-based p38 MAP kinase inhibitors via [3+2]-cycloaddition chemistry," New Journal of Chemistry, vol. 331010-1016, no. 5, pp. 1010-1016, 2009.
[42]
C. Dyrager et al., "Synthesis and Photophysical Characterisation of Fluorescent 8-(1H-1,2,3-Triazol-4-yl)adenosine Derivatives," European Journal of Organic Chemistry, no. 10, pp. 1515-1521, 2009.
[43]
M. Klein et al., "Synthesis of 3-(1,2,3-triazol-1-yl)- and 3-(1,2,3-triazol-4-yl)-substituted pyrazolo[3,4-d]pyrimidin-4-amines via click chemistry : potential inhibitors of the Plasmodium falciparum PfPK7 protein kinase," Organic and biomolecular chemistry, vol. 7, no. 17, pp. 3421-3429, 2009.
[44]
M. Klein et al., "Synthesis of chiral 1,4-disubstituted-1,2,3-triazole derivatives from amino acids," Molecules, vol. 14, no. 12, pp. 5124, 2009.
[45]
P. Dinér et al., "On the origin of the stereoselectivity in organocatalysed reactions with trimethylsilyl-protected Diarylprolinol," Chemistry - A European Journal, vol. 14, no. 1, pp. 122-127, 2008.
[46]
M. Nielsen et al., "ORGN 12-Asymmetric organocatalytic heteroatomic alpha- and beta-functionalizations of alpha,beta-unsaturated electrophiles," in Abstracts of Papers of the American Chemical Society, 2008.
[47]
M. Nielsen et al., "ORGN 703-Two diverse approaches for asymmetric organocatalytic beta-hydroxylation of alpha,beta-unsaturated electrophiles," in Abstracts of Papers of the American Chemical Society, 2008.
[48]
S. Bertelsen et al., "Asymmetric organocatalytic beta-hydroxylation of alpha, beta-unsaturated aldehydes," Journal of the American Chemical Society, vol. 129 1536-1537, no. 6, pp. 1536-1537, 2007.
[49]
P. Dinér et al., "Enantioselective hydroxylation of nitroalkenes : an organocatalytic approach," Chemical Communications, no. 35, pp. 3646-3648, 2007.
[50]
P. Dinér et al., "Enantioselective organocatalytic conjugate addition of N heterocycles to alpha,beta-unsaturated aldehydes," Angewandte Chemie International Edition, vol. 46, no. 12, pp. 1983-1987, 2007.