A Step‐Economic Synthesis of (S)‐(−)‐Juglomycin C and (S)‐(−)‐NHAB by Dötz Benzannulation and Convergent Deprotections (original) (raw)

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Intra- and Intermolecular Oxa-Pictet-Spengler Cyclization Strategy for the ­Enantioselective Synthesis of Deoxy Analogues of (+)-Nanomycin A Methyl Ester, (+)-Eleutherin, (+)-Allo-Eleutherin, and (+)-Thysanone

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European Journal of Organic Chemistry, 2010

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A Four-Component Domino Reaction: An Eco-Compatible and Highly Efficient Construction of 1,8-Naphthyridine Derivatives, Their In Silico Molecular Docking, Drug Likeness, ADME, and Toxicity Studies

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The synthesis of 7-carbonyl homologues of 1-deoxynojirimycin

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SYNTHESIS OF NOVEL 2-AMINO-5,7-DIMETHYL-8-[1,8] NAPHTHYRIDINE-2-YL-4-ARYL-QUINOLINE-3-CARBONITRILES Via ONE-POT CONDENSATION

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Tetrahedron Letters, 1999

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Base promoted facile route to functionalized benzo[b][1,8]naphthyridin-2-(1H)-ones from N-benzyl-N-(3-cyanoquinolin-2-yl)acetamides

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