Works matching IS 13811991 AND DT 2018 AND VI 22 AND IP 2
Results: 15
Design, synthesis, and SAR study of highly potent, selective, irreversible covalent JAK3 inhibitors.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 343, doi. 10.1007/s11030-017-9803-2
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Nucleophilic ring opening reactions of aziridines.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 447, doi. 10.1007/s11030-018-9829-0
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Ultrasound-assisted reaction of 1,4-naphthoquinone with anilines through an EDA complex.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 281, doi. 10.1007/s11030-018-9820-9
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A new computational model for the prediction of toxicity of phosphonate derivatives using QSPR.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 269, doi. 10.1007/s11030-018-9819-2
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Exploring the chemical space of peptides for drug discovery: a focus on linear and cyclic penta-peptides.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 259, doi. 10.1007/s11030-018-9812-9
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Recent advances in the development of polycyclic skeletons via Ugi reaction cascades.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 503, doi. 10.1007/s11030-017-9811-2
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Synthesis of sulfur-containing heterocycles via ring enlargement.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 517, doi. 10.1007/s11030-017-9810-3
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A green non-acid-catalyzed process for direct N=N-C group formation: comprehensive study, modeling, and optimization.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 335, doi. 10.1007/s11030-017-9808-x
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Recent developments in the synthesis and applications of dihydropyrimidin-2(1H)-ones and thiones.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 405, doi. 10.1007/s11030-017-9806-z
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Synthesis and structure-activity relationship study of diaryl[d,f][1,3]diazepines as potential anti-cancer agents.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 323, doi. 10.1007/s11030-017-9805-0
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An integrated structure- and pharmacophore-based MMP-12 virtual screening.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 383, doi. 10.1007/s11030-017-9804-1
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One-pot synthesis of novel 1-(1H-tetrazol-5-yl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine derivatives via an Ugi-azide 4CR process.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 291, doi. 10.1007/s11030-017-9801-4
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QSPR analysis of threshold of odor for the large number of heterogenic chemicals.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 397, doi. 10.1007/s11030-017-9800-5
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Synthesis and evaluation of bile acid amides of α-cyanostilbenes as anticancer agents.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 305, doi. 10.1007/s11030-017-9797-9
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Application of two-dimensional binary fingerprinting methods for the design of selective Tankyrase I inhibitors.
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- Molecular Diversity, 2018, v. 22, n. 2, p. 359, doi. 10.1007/s11030-017-9793-0
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