Publications

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Publications

[2]
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.
[3]
B. Blomkvist and P. Dinér, "Mild and Rapid Aniline/HBF4•DEE‐Catalysed Formation of Sulfinyl Imines," ChemistrySelect, 2019.
[4]
B. Blomkvist et al., "Student-Driven Development of Greener Chemistry in Undergraduate Teaching: Synthesis of Lidocaine Revisited," Journal of Chemical Education, pp. 1389-1394, 2019.
[5]
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.
[6]
B. Blomkvist and P. Dinér, "HBF4·DEE-catalyzed formation of sulfinyl imines: Synthesis and mechanistic studies," Tetrahedron Letters, vol. 59, pp. 1249-1253, 2018.
[7]
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.
[9]
L. Wang et al., "A Nickel (II) PY5 Complex as an Electrocatalyst for Water Oxidation," Journal of Catalysis, vol. 335, pp. 72-78, 2016.
[11]
P. Dinér, "Yttrium from Ytterby," Nature Chemistry, vol. 8, no. 2, pp. 192-192, 2016.
[12]
[13]
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.
[14]
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.
[15]
P. Dinér, A. Sadhukhan and B. Blomkvist, "Chiral Sulfinamides as Highly Enantioselective Organocatalysts," ChemCatChem, vol. 6, no. 11, pp. 3063-3066, 2014.
[16]
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.
[18]
J.-F. Poon et al., "Azastilbenes : a cut-off to p38 MAPK inhibitors," Organic and biomolecular chemistry, vol. 11, no. 27, 2013.
[19]
J. J. Verendel and P. Dinér, "Efficient, Low Temperature Production of Hydrogen from Methanol," ChemCatChem, vol. 5, no. 10, pp. 2795-2797, 2013.
[20]
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.
[21]
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.
[22]
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.
[23]
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.
[24]
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.
[25]
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.
[26]
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.
[27]
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.
[28]
C. Dyrager et al., "Design, synthesis, and biological evaluation of chromone-based p38 MAP kinase inhibitors," Journal of Medicinal Chemistry, vol. 54, 2011.
[30]
[31]
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.
[32]
[33]
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.
[34]
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.
[35]
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.
[37]
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.
[38]
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.
[39]
[40]
[41]
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.
[42]
P. Dinér et al., "Enantioselective hydroxylation of nitroalkenes : an organocatalytic approach," Chemical Communications, no. 35, pp. 3646-3648, 2007.
[43]
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.
[44]
P. Dinér and M. Amedjkouh, "Aminophosphonates as organocatalysts in the direct asymmetric aldol reaction towards syn selectivity in the presence of Lewis bases," Organic and biomolecular chemistry, vol. 4, no. 11, pp. 2091-2096, 2006.
[45]
S. Bertelsen et al., "Dienamine catalysis : organocatalytic asymmetric gamma-amination of alpha,beta-unsaturated aldehydes," Journal of the American Chemical Society, vol. 128, no. 39, pp. 12973-12980, 2006.
Page responsible:Peter Dinér
Belongs to: Department of Chemistry
Last changed: Jun 02, 2017