LEADER 01150cam0 2200241 450 001 E600200031554 005 20210927082352.0 100 $a20071116d2004 |||||ita|0103 ba 101 $aita 102 $aIT 200 1 $aAtti della XXXVII riunione scientifica$ePreistoria e Protostoria della Calabria, Scalea, Papasidero, Praia a Mare, Tortora, 29 settembre - 4 ottobre 2002$fIstituto Italiano di Preistoria e Protostoria 210 $aFirenze$cIstituto Italiano di Preistoria e Protostoria$d2004 215 $a2 v.$d24 cm. 710 02$a*Istituto italiano di Preistoria e Protostoria$3A600200044690$4070$0387152 801 0$aIT$bUNISOB$c20210927$gRICA 850 $aUNISOB 852 $aUNISOB$jLaboratorio|Archeologico$m136498-136499 912 $aE600200031554 940 $aM 102 Monografia moderna SBN 941 $aM 957 $aLaboratorio|Archeologico$b000340$i-1-2$gCON$d136498-136499$racquisto Laboratorio archeologico$1catenacci$2UNISOB$3UNISOB$420071116082939.0$520210927082342.0$6Spinosa$fModalità di consultazione vedi home page della Biblioteca link Fondi 996 $aAtti della XXXVII riunione scientifica$91687636 997 $aUNISOB LEADER 01380nas 2200457-a 450 001 996208032603316 005 20230222213018.0 035 $a(OCoLC)60623087 035 $a(CKB)954921420515 035 $a(CONSER)--2007228706 035 $a(EXLCZ)99954921420515 100 $a20050614a19919999 --- - 101 0 $aeng 135 $aur||||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aJournal of legal economics 210 $a[Florence, Ala.] $cAmerican Academy of Economic and Financial Experts 300 $aRefereed/Peer-reviewed 311 $a1054-3023 517 1 $aLegal economics 517 1 $aJ. Legal Econ 606 $aForensic economics$vPeriodicals 606 $aForensic economics$zUnited States$vPeriodicals 606 $aForensic economics$2fast$3(OCoLC)fst00931959 606 $aRechtseconomie$2gtt 607 $aUnited States$2fast 608 $aPeriodicals.$2fast 608 $aPeriodicals.$2lcgft 615 0$aForensic economics 615 0$aForensic economics 615 7$aForensic economics. 615 17$aRechtseconomie. 676 $a346.7303/23 676 $a347.306323 712 02$aAmerican Academy of Economic and Financial Experts. 906 $aJOURNAL 912 $a996208032603316 996 $aJournal of legal economics$92180739 997 $aUNISA LEADER 05154nam 2200589 a 450 001 9910830708303321 005 20230617035343.0 010 $a1-280-51959-2 010 $a9786610519590 010 $a3-527-60393-X 010 $a3-527-60419-7 035 $a(CKB)1000000000376383 035 $a(EBL)482113 035 $a(OCoLC)68623535 035 $a(SSID)ssj0000204331 035 $a(PQKBManifestationID)11172942 035 $a(PQKBTitleCode)TC0000204331 035 $a(PQKBWorkID)10176359 035 $a(PQKB)10538143 035 $a(MiAaPQ)EBC482113 035 $a(EXLCZ)991000000000376383 100 $a20041018d2004 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aModern fluoroorganic chemistry$b[electronic resource] $esynthesis, reactivity, applications /$fPeer Kirsch 210 $aWeinheim $cWiley-VCH$dc2004 215 $a1 online resource (322 p.) 300 $aDescription based upon print version of record. 311 $a3-527-30691-9 320 $aIncludes bibliographical references and index. 327 $aModern Fluoroorganic Chemistry; Contents; Preface; List of Abbreviations; 1 Introduction; 1.1 Why Organofluorine Chemistry?; 1.2 History; 1.3 The Basic Materials; 1.3.1 Hydrofluoric Acid; 1.3.2 Fluorine; 1.4 The Unique Properties of Organofluorine Compounds; 1.4.1 Physical Properties; 1.4.2 Chemical Properties; 1.4.3 Ecological Impact; 1.4.3.1 Ozone Depletion by Chlorofluorocarbons; 1.4.3.2 Greenhouse Effect; 1.4.4 Physiological Properties; 1.4.5 Analysis of Fluorochemicals: (19)F NMR Spectroscopy; 2 Synthesis of Complex Organofluorine Compounds; 2.1 Introduction of Fluorine 327 $a2.1.1 Perfluorination and Selective Direct Fluorination2.1.2 Electrochemical Fluorination (ECF); 2.1.3 Nucleophilic Fluorination; 2.1.3.1 Finkelstein Exchange; 2.1.3.2 "Naked" Fluoride; 2.1.3.3 Lewis Acid-assisted Fluorination; 2.1.3.4 The "General Fluorine Effect"; 2.1.3.5 Amine-Hydrogen Fluoride and Ether-Hydrogen Fluoride Reagents; 2.1.3.6 Hydrofluorination, Halofluorination, and Epoxide Ring Opening; 2.1.4 Synthesis and Reactivity of Fluoroaromatic Compounds; 2.1.4.1 Synthesis of Fluoroaromatic Compounds; 2.1.4.2 Reductive Aromatization; 2.1.4.3 The Balz-Schiemann Reaction 327 $a2.1.4.4 The Fluoroformate Process2.1.4.5 Transition Metal-assisted Oxidative Fluorination; 2.1.4.6 The Halex Process; 2.1.4.7 Think Negative! - "Orthogonal" Reactivity of Perfluoroaromatic and Perfluoroolefinic Systems; 2.1.4.8 The "Special Fluorine Effect"; 2.1.4.9 Aromatic Nucleophilic Sustitution; 2.1.4.10 Activation of the Carbon-Fluorine Bond by Transition Metals; 2.1.4.11 Activation of Fluoroaromatic Compounds by ortho-Metalation; 2.1.5 Transformations of Functional Groups; 2.1.5.1 Hydroxy into Fluoro; 2.1.5.2 Conversion of Carbonyl into gem-Difluoromethylene 327 $a2.1.5.3 Carboxyl into Trifluoromethyl2.1.5.4 Oxidative Fluorodesulfuration; 2.1.6 "Electrophilic" Fluorination; 2.1.6.1 Xenon Difluoride; 2.1.6.2 Perchloryl Fluoride and Hypofluorides; 2.1.6.3 "NF"-Reagents; 2.2 Perfluoroalkylation; 2.2.1 Radical Perfluoroalkylation; 2.2.1.1 Structure, Properties, and Reactivity of Perfluoroalkyl Radicals; 2.2.1.2 Preparatively Useful Reactions of Perfluoroalkyl Radicals; 2.2.1.3 "Inverse" Radical Addition of Alkyl Radicals to Perfluoroolefins; 2.2.2 Nucleophilic Perfluoroalkylation; 2.2.2.1 Properties, Stability, and Reactivity of Fluorinated Carbanions 327 $a2.2.2.2 Perfluoroalkyl Metal Compounds2.2.2.3 Perfluoroalkyl Silanes; 2.2.3 "Electrophilic" Perfluoroalkylation; 2.2.3.1 Properties and Stability of Fluorinated Carbocations; 2.2.3.2 Aryl Perfluoroalkyl Iodonium Salts; 2.2.3.3 Perfluoroalkyl Sulfonium, Selenonium, Telluronium, and Oxonium Salts; 2.2.4 Difluorocarbene and Fluorinated Cyclopropanes; 2.3 Selected Fluorinated Structures and Reaction Types; 2.3.1 Difluoromethylation and Halodifluoromethylation; 2.3.2 The Perfluoroalkoxy Group; 2.3.3 The Perfluoroalkylthio Group and Sulfur-based Super-electron-withdrawing Groups 327 $a2.3.4 The Pentafluorosulfuranyl Group and Related Structures 330 $aIn this handbook, Peer Kirsch clearly shows that this exciting field is no longer an exotic area of research. Aimed primarily at synthetic chemists wanting to gain a deeper understanding of the fascinating implications of including the highly unusual element fluorine in organic compounds, the main part of the book presents a wide range of synthetic methodologies and the experimental procedures selected undeniably show that this can be done with standard laboratory equipment. To round off, the author looks at fluorous chemistry and the applications of organofluorine compounds in liquid crystals 606 $aOrganofluorine compounds 615 0$aOrganofluorine compounds. 676 $a547.02 676 $a547.6 700 $aKirsch$b Peer$01606153 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830708303321 996 $aModern fluoroorganic chemistry$93931795 997 $aUNINA