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Hydrocarbons --- Oxidation --- Palladium catalysts

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"Palladium-Catalyzed Modification of Nucleosides, Nucleotides and Oligonucleotides describes the procedures and protocols related to the modification of nucleosides, nucleotides and oligonucleotides via Pd-mediated cross-coupling processes. The book highlights the growing area of nucleic acid modification and how Pd-mediated coupling reactions can assist this development. Users will find key synthetic protocols for these reactions in this latest volume in the Latest Trends in Palladium Chemistry series. As most of the research in the field of antiviral agents has centered on the use of modified nucleosides that have exhibited promising activity, this book provides an up-to-date reference for both professionals in industry and other interested parties" -- elsevier.com.

Palladium catalysts. --- Nucleosides. --- Nucleotides. --- Phosphonucleosides --- Nucleic acids --- Nucleotides --- Catalysts

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Organic compounds --- Palladium catalysts --- Composés organiques --- Palladium --- Synthesis --- Synthèse --- Catalyseurs --- Palladium catalysts. --- Synthesis. --- -Palladium catalysts --- #WSCH:LOSH --- Catalysts --- Compounds, Organic --- Organic chemicals --- Carbon compounds --- Composés organiques --- Synthèse --- Chemistry, Organic --- Chemistry, Synthetic organic --- Organic synthesis (Chemistry) --- Synthetic organic chemistry --- Organic compounds - Synthesis.

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Organic compounds --- Palladium catalysts --- #WSCH:LOSH --- 547.057 --- Catalysts --- Chemistry, Organic --- Chemistry, Synthetic organic --- Organic synthesis (Chemistry) --- Synthetic organic chemistry --- 547.057 Organic chemistry--?.057 --- Organic chemistry--?.057 --- Synthesis --- Information Technology --- Computer Science (Hardware & Networks) --- Organic compounds - Synthesis

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The author has developed novel methodologies for highly efficient construction of functionalized heterocycles by palladium-catalyzed domino/cascade cyclization of allenes and related compounds containing appropriate nucleophilic group(s). Based on these methodologies, enantioselective total syntheses of bioactive natural products, pachastrissamine (26% overall yield in seven steps), lysergic acid (4.0% overall yield in fifteen steps), lysergol (3.6% overall yield in fifteen steps) and isolysergol (8.2% overall yield in eleven steps) have been achieved. These are more facile synthetic route than those previously reported. These findings would contribute to the development of efficient synthetic methods for biologically active compounds containing a complex structure.

Bioactive compounds -- Synthesis. --- Chemistry. --- Palladium catalysts. --- Bioactive compounds --- Palladium catalysts --- Human Anatomy & Physiology --- Chemistry --- Health & Biological Sciences --- Physical Sciences & Mathematics --- Organic Chemistry --- Animal Biochemistry --- Synthesis --- Ring formation (Chemistry) --- Synthesis. --- Biologically active compounds --- Compounds, Bioactive --- Compounds, Biologically active --- Compounds, Physiologically active --- Physiologically active compounds --- Cyclization (Chemistry) --- Cycloaddition --- Exo-condensation --- Bioorganic chemistry. --- Catalysis. --- Bioorganic Chemistry. --- Chemical reactions --- Catalysts --- Chemicals --- Activation (Chemistry) --- Chemistry, Physical and theoretical --- Surface chemistry --- Bio-organic chemistry --- Biological organic chemistry --- Biochemistry --- Chemistry, Organic