Search Results - "Wagger, Jernej"
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Regioselective Synthesis of 5- and 3-Hydroxy-N-Aryl-1H-Pyrazole-4-Carboxylates and Their Evaluation as Inhibitors of Plasmodium falciparum Dihydroorotate Dehydrogenase
Published in Molecules (Basel, Switzerland) (25-07-2022)“…In silico evaluation of various regioisomeric 5- and 3-hydroxy-substituted alkyl 1-aryl-1H-pyrazole-4-carboxylates and their acyclic precursors yielded…”
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A synthesis of 1-substituted 5-[2-(acylamino)ethyl]-1H-pyrazole-4-carboxamides
Published in Tetrahedron (22-08-2009)Get full text
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Synthesis of 3-(2-aminoethyl)-5-hydroxy-1H-pyrazole derivatives
Published in ARKIVOC (01-01-2012)Get full text
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Synthesis of ( S, Z)-3-[(1 H-indol-3-yl)methylidene]hexahydropyrrolo[1,2- a]pyrazin-4(1 H)-one: an alternative, enaminone based, route to unsaturated cyclodipeptides
Published in Tetrahedron (17-03-2008)“…A series of racemic and enantiopure ( S, Z)-3-[(1 H-indol-3-yl)methylidene]hexahydropyrrolo[1,2- a]pyrazin-4(1 H)-one (cyclic Pro–ΔTrp) dipeptide analogues…”
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Tetrahydro-1H,5H-pyrazolo[1,2-a]pyrazole-1-carboxylates as inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase
Published in Bioorganic chemistry (01-08-2019)“…[Display omitted] •Novel 3D-rich scaffold among PfDHODH inhibitors.•Simple synthetic method, broad scope, separable diastereomers.•Separable diastereomers,…”
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[2+2] Cycloaddition of electron-poor acetylenes to ( E)-3-dimethylamino-1-heteroaryl-prop-2-en-1-ones: synthesis of highly functionalized 1-heteroaroyl-1,3-butadienes
Published in Tetrahedron letters (30-06-2010)“…Microwave-assisted [2+2] cycloaddition of ( E)-3-dimethylamino-1-heteroaryl-prop-2-en-1-ones to dimethyl acetylenedicarboxylates gives (2 E,3…”
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A Constrained Tricyclic Nucleic Acid Analogue of α‑l‑LNA: Investigating the Effects of Dual Conformational Restriction on Duplex Thermal Stability
Published in Journal of organic chemistry (20-09-2013)“…A constrained tricyclic analogue of α-l-LNA (2), which contains dual modes of conformational restriction about the ribose sugar moiety, has been synthesized…”
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The effect of substituents on the chiral solvating properties of ( S)-1,6-dialkylpiperazine-2,5-diones
Published in Tetrahedron: asymmetry (30-06-2011)“…The effect of substituents on the chiral solvating properties of 13 different ( S)-1,6-dialkylpiperazine-2,5-diones ( S)- 1a– m and five (3 S,6…”
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Chiral solvating properties of ( S)-1-benzyl-6-methylpiperazine-2,5-dione
Published in Tetrahedron: asymmetry (12-03-2007)“…In CDCl 3 solution, enantiopure ( S)-1-benzyl-6-methylpiperazine-2,5-dione ( S)- 1a formed diastereomeric C O⋯ H–N hydrogen-bonded associates with racemic (…”
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( S)- N-Benzyl-3(6)-methylpiperazine-2,5-diones as chiral solvating agents for N-acylamino acid esters
Published in Tetrahedron: asymmetry (11-07-2008)“…Three closely related diketopiperazines, ( S)-1-benzyl-6-methylpiperazine-2,5-dione ( S)- 1a, ( S)-1-benzyl-3-methylpiperazine-2,5-dione ( S)- 1b, and (…”
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Enaminone-Based Synthesis of Dipodazine Derivatives
Published in Helvetica chimica acta (01-02-2006)“…A series of racemic dipodazine analogues 9 were prepared in 22–80% yield from…”
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Synthesis and structure of novel ( S)-1,6-dialkylpiperazine-2,5-diones and (3 S,6 S)-1,3,6-trialkylpiperazine-2,5-diones
Published in Tetrahedron: asymmetry (30-03-2011)“…Eleven ( S)-1,6-dialkylpiperazine-2,5-diones and five (3 S,6 S)-1,3,6-trialkylpiperazine-2,5-diones were prepared in three steps from the corresponding (…”
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13
A synthesis of 1-substituted 5-[2-(acylamino)ethyl]-1 H-pyrazole-4-carboxamides
Published in Tetrahedron (2009)“…A seven-step synthesis of 1-substituted 5-(2-acylaminoethyl)-1 H-pyrazole-4-carboxamides 20 as the pyrazole analogues of histamine was developed. The synthesis…”
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Parallel Solution-Phase Synthesis of (Z)-3-(Arylamino)-2,3-dehydroalanine Derivatives and Solid-Phase Synthesis of Fused Pyrimidones
Published in Journal of combinatorial chemistry (01-05-2004)“…N-Protected (Z)-3-(arylamino)-2,3-dehydroalanine esters 5 and 10 were prepared in one step from methyl (Z)-2-acylamino-3-(dimethylamino)prop-2-enoates 3 and 9…”
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