Works matching IS 13811991 AND DT 2012 AND VI 16 AND IP 3
Results: 19
Applications of ortho-phenylisonitrile and ortho- N-Boc aniline for the two-step preparation of novel bis-heterocyclic chemotypes.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 607, doi. 10.1007/s11030-012-9374-1
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Synthesis of peptidomimetics, δ- and $${\varepsilon}$$-lactam tetrazoles.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 601, doi. 10.1007/s11030-012-9373-2
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Novel ionic liquid supported-multicomponent reaction toward chimeric bis-heterocycles.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 503, doi. 10.1007/s11030-012-9383-0
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A novel and efficient one-pot four-component tandem approach for the synthesis of pyran derivatives.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 423, doi. 10.1007/s11030-012-9375-0
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- Article
A facile three- and four-component procedure toward the synthesis of functionalized pyrano- and benzo[ f]quinoxaline derivatives.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 453, doi. 10.1007/s11030-012-9379-9
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Sensitive electrospray mass spectrometry analysis of one-bead-one-compound peptide libraries labeled by quaternary ammonium salts.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 613, doi. 10.1007/s11030-012-9377-y
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- Article
An efficient three-component, one-pot synthesis of 2-alkylthio-4-amino-5-cyano-6-aryl(alkyl)pyrimidines in water.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 431, doi. 10.1007/s11030-012-9376-z
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In silico design of peptidic inhibitors targeting estrogen receptor alpha dimer interface.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 441, doi. 10.1007/s11030-012-9378-x
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Exploring a sulfone linker utilizing trimethyl aluminum as a cleavage reagent: solid-phase synthesis of sulfonamides and ureas.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 463, doi. 10.1007/s11030-012-9380-3
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Syntheses of novel diaryl[ d, f ][1,3]diazepines via one-pot Suzuki coupling followed by direct ring closure with carboxylic acids.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 489, doi. 10.1007/s11030-012-9382-1
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Focused enumeration and assessing the structural diversity of scaffold libraries: conformationally restricted bicyclic secondary diamines.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 477, doi. 10.1007/s11030-012-9381-2
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Consensus QSAR model for identifying novel H5N1 inhibitors.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 513, doi. 10.1007/s11030-012-9384-z
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Ultrasound-promoted synthesis and immunosuppressive activity of novel quinazoline derivatives.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 579, doi. 10.1007/s11030-012-9390-1
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Rationalizing lead optimization by consensus 2D- CoMFA CoMSIA GRIND (3D) QSAR guided fragment hopping in search of γ-secretase inhibitors.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 563, doi. 10.1007/s11030-012-9388-8
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Sustainable synthesis and automated deposition: an accessible discovery screening library of fragment-like purines.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 541, doi. 10.1007/s11030-012-9386-x
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Synthesis and evaluation of functionalized indoles as antimycobacterial and anticancer agents.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 525, doi. 10.1007/s11030-012-9385-y
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A rational approach to selective pharmacophore designing: an innovative strategy for specific recognition of Gsk3β.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 553, doi. 10.1007/s11030-012-9387-9
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Reaction between enaminones and acetylenic esters in the presence of triphenylphosphine: a convenient synthesis of alkyl 2(1-benzyl-2,4-dioxo-2,3,4,5,6,7-hexahydro-1 H-indol-3-yl)acetates.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 619, doi. 10.1007/s11030-012-9389-7
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Regioselective multi-component synthesis of 1 H-pyrazolo[3,4- d]pyrimidine-6(7 H)-thiones.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 591, doi. 10.1007/s11030-012-9391-0
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