LEADER 05419nam 2200697Ia 450 001 9910458756903321 005 20200520144314.0 010 $a1-280-63285-2 010 $a9786610632855 010 $a0-08-045563-8 024 3 $z9780080444741 035 $a(CKB)1000000000365293 035 $a(EBL)269566 035 $a(OCoLC)171134062 035 $a(SSID)ssj0000099221 035 $a(PQKBManifestationID)11132894 035 $a(PQKBTitleCode)TC0000099221 035 $a(PQKBWorkID)10007152 035 $a(PQKB)11477286 035 $a(MiAaPQ)EBC269566 035 $a(PPN)159637279 035 $a(Au-PeEL)EBL269566 035 $a(CaPaEBR)ebr10137941 035 $a(CaONFJC)MIL63285 035 $a(OCoLC)162567857 035 $a(EXLCZ)991000000000365293 100 $a20050302d2006 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aAdvances in synthetic organic chemistry and methods reported in US patents$b[electronic resource] /$fThomas F. DeRosa 210 $aAmsterdam ;$aBoston ;$aLondon $cElsevier$d2006 215 $a1 online resource (705 p.) 300 $aDescription based upon print version of record. 311 $a0-08-044474-1 320 $aIncludes bibliographical references and index. 327 $afront 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 327 $aHalogenated 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 327 $a4-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 327 $aCarboxamide 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 327 $aSubstituted 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 327 $aAza and Diaza Bi-and Tricyclics 330 $a 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 606 $aOrganic compounds$xSynthesis 606 $aOrganic compounds$xSynthesis$vPatents 606 $aPatents$zUnited States 608 $aElectronic books. 615 0$aOrganic compounds$xSynthesis. 615 0$aOrganic compounds$xSynthesis 615 0$aPatents 676 $a547.2 700 $aDeRosa$b Thomas F$0863953 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910458756903321 996 $aAdvances in synthetic organic chemistry and methods reported in US patents$91928569 997 $aUNINA