Advances in synthetic organic chemistry and methods reported in US patents [[electronic resource] /] / Thomas F. DeRosa

• Autore: DeRosa Thomas F
• Pubblicazione: Amsterdam ; ; Boston ; ; London, : Elsevier, 2006
• Descrizione fisica: 1 online resource (705 p.)
• Disciplina: 547.2
• Soggetto topico: Organic compounds - Synthesis; Patents - United States
• Soggetto genere / forma: Electronic books.
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references and index.
• Nota di contenuto: front cover; copyright; table of contents; front matter; Introduction; body; Acids and Derivatives; Aromatic Carboxylic Acid Derivatives; Azinyloxy,and Phenoxy-Diaryl-Carboxylic Acid Derivatives, Their Preparation and Use as Mixed ETA/ETB Endothelin Receptor Antagonists; Cinnamic Acid Derivatives; Compounds Derived from Benzoic Acid Esters,Composition Containing Said Compounds and Use Thereof; 1,2-Diarylmethylene Derivatives, Their Methods of Preparation, and Their Uses in Therapeutics; Geranic Acid Derivatives ; Halogenated Cinnamic Acids and Esters Thereof, Processes for the Preparation Thereof and Halogenated Aryldiazonium SaltsHalogenation Catalyst; Method for Producing Alkoxy Malonic Acid Dinitriles; Phosphonosuccinic Acid Derivatives, Processes for Their Preparation and Medicaments Containing These Compounds; Preparation of Cyclohexane Carboxylate Derivatives; Water Soluble Fullerenes with Antiviral Activity; Alcohols; Butyne Diol Derivatives; 1,2-Dithin Antiinfective Agents; Oligiocycloalkanoid Compounds and Methods of Use; Polymers with Controlled Physical State and Bioerodibility ; 4-Quinolinemethanol Derivatives as Purine Receptor AntagonistsSynthesis of 5-Decenyl Acetate and Other Pheromone Components; Aldols; Stereospecific Synthesis of Aldols; Aldehydes; Process for Selective Catalytic Oxidation of Olefins to Aldehydes, Ketones with Cleavage of C==C Bonds; Alkenes; Carbonyl-Containing Compounds; Alkynes; Diaryl-enynes; DNA-Cleaving Anti-Tumor Agents; Amides; Adamantane Derivatives; o-Anisamide Derivatives; Benzamide Analogues Useful as PARP (ADP-Ribosyltransferase, ADPRT) DNA Repair Enzyme Inhibitors ; Carboxamide Compositions, Methods, and Compositions for Inhibiting PARP ActivityHeterocyclic Amides; Phosphoramide Compounds; Amines; Aminophenyl Ketones Derivatives and a Method for the Preparation Thereof; Arylamine Synthesis; Fungicidal Spirocyclic Amines; Method for Producing Propargylamine Compounds; One Pot Process for the Preparation of 1-[2-Methylamino-(4-Methoxyphenyl)-Ethyl]Cyclohexanol; Organic Electroluminescence Device and Phenylenediamine Derivative; Process for Preparing N-Substituted Hydroxylamines and Salts Thereof; Sodium Channel Modulators ; Substituted 2-Aminoalkyl 1,4-Diaminobenzene Compounds and Oxidation Dye Precursor Containing the SameAminoacids; Aminoindanes; Aminopropylphosphinic Acids; Cyclic Aminoacids and Derivatives Thereof Useful as Pharmaceutical Agents; Isocyanoalkyl, Carbonic Acid Derivatives, Their Conversion into Secondary Amidoalkyl Carbonic Acid Derivatives by Isocyanide Multicomponent Reactions, as well as these Secondary Amidoalkyl Carbonic Acid Derivatives; Spirodiamino Acid Scaffold for Combinatorial Synthesis; Anthracenones; 10-Substituted 1,8-Dihydroxy-9(10H) Anthracenone Pharmaceuticals ; Aza and Diaza Bi-and Tricyclics
• Sommario/riassunto: Advances in Synthetic Organic Chemistry and Methods Reported in US Patents provides synthetic guidelines for preparing current and commercially significant organic compounds, derivatives, and intermediates as reported in issued US Patents. Industries surveyed include agrochemical, cosmetics and personal care products. Each entry contains extensive information such as explicit laboratory directions for preparing all chemical intermediates and characterization data. Furthermore, product optimization studies, industrial preparation, and new synthetic methods have been included for select
• Titolo autorizzato: Advances in synthetic organic chemistry and methods reported in US patents
• ISBN: 1-280-63285-2; 9786610632855; 0-08-045563-8
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910458756903321
• Lo trovi qui: Univ. Federico II