LEADER 00857nam0-2200313---450- 001 990009823730403321 005 20140217121139.0 010 $a88-14-16918-7 035 $a000982373 035 $aFED01000982373 035 $a(Aleph)000982373FED01 035 $a000982373 100 $a20140217d2012----km-y0itay50------ba 101 0 $aita 102 $aIT 105 $ay-------001yy 200 1 $aDei legittimari$e[Artt. 536-564]$fAndrea Bucelli 210 $aMilano$cGiuffrč$d©2012 215 $aXXII, 839 p.$d24 cm 225 1 $a<>Codice civile. Commentario 676 $a346.4505202638$v21$zita 700 1$aBucelli,$bAndrea$0260143 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990009823730403321 952 $aVIII B 642 (119)$b55339*$fFGBC 959 $aFGBC 996 $aDei legittimari$9835418 997 $aUNINA LEADER 01150nam a2200277 i 4500 001 991001968929707536 008 130226s2007 enk b 001 0 eng d 020 $a9780754657132 035 $ab14100083-39ule_inst 040 $aDip.to Studi Umanistici - Sez. Filologia Classica e Sc. Filosofiche$bita 082 $a261 100 1 $aKahlos, Maijastina$0285264 245 10$aDebate and dialogue :$bchristian and pagan cultures c. 360-430 /$cMaijastina Kahlos 260 $aAldershot ;$aBurlington, VT :$bAshgate,$c2007 300 $aX, 213 p. ;$c24 cm 440 0$aAshgate new critical thinking in religion, theology, and biblical studies. 504 $aBibliografia: p. [185]-203. Indice 650 4$aApologetica$xChiesa primitiva 650 4$aCristianesimo e religioni non cristiane$zImpero romano 651 4$aReligione romana 907 $a.b14100083$b03-03-14$c26-02-13 912 $a991001968929707536 945 $aLE007 261 KAH 01.01$g1$i2007000239179$lle007$op$pE63.25$q-$rl$s- $t0$u0$v0$w0$x0$y.i15486047$z01-03-13 996 $aDebate and dialogue$9265428 997 $aUNISALENTO 998 $ale007$b26-02-13$cm$da $e-$feng$genk$h0$i0 LEADER 04358nam 2200589 450 001 9910827921703321 005 20200520144314.0 010 $a1-118-75498-0 010 $a1-118-75495-6 010 $a1-118-75488-3 035 $a(CKB)3710000000521830 035 $a(EBL)4182965 035 $a(MiAaPQ)EBC4182965 035 $a(DLC) 2015025134 035 $a(Au-PeEL)EBL4182965 035 $a(CaPaEBR)ebr11125572 035 $a(CaONFJC)MIL878185 035 $a(OCoLC)932334514 035 $a(PPN)250378035 035 $a(EXLCZ)993710000000521830 100 $a20160105h20162016 uy 0 101 0 $aeng 135 $aur||||||||||| 181 $2rdacontent 182 $2rdamedia 183 $2rdacarrier 200 00$aArene chemistry $ereaction mechanisms and methods for aromatic compounds /$fedited by Jacques Mortier 210 1$aHoboken, New Jersey :$cWiley,$d2016. 210 4$d©2016 215 $a1 online resource (990 p.) 300 $aIncludes index. 311 $a1-118-75201-5 320 $aIncludes bibliographical references and index. 327 $aTITLE PAGE ; COPYRIGHT PAGE ; CONTENTS; LIST OF CONTRIBUTORS; PREFACE; Part I Electrophilic Aromatic Substitution ; CHAPTER 1 ELECTROPHILIC AROMATIC SUBSTITUTION: MECHANISM ; 1.1 INTRODUCTION; 1.2 GENERAL ASPECTS; 1.3 ELECTROPHILES; 1.4 ARENE NUCLEOPHILES; 1.5 ?-COMPLEX INTERMEDIATES ; 1.6 ?-COMPLEX OR WHELAND INTERMEDIATES ; 1.7 SUMMARY AND OUTLOOK; ABBREVIATIONS ; REFERENCES ; CHAPTER 2 FRIEDEL-CRAFTS ALKYLATION OF ARENES IN TOTAL SYNTHESIS ; 2.1 INTRODUCTION; 2.2 TOTAL SYNTHESIS INVOLVING INTERMOLECULAR FC ALKYLATIONS; 2.2.1 Synthesis of Coenzyme Q10 327 $a2.2.2 Total Synthesis of (±)-Brasiliquinone B 2.2.3 Synthesis of (2212;)-Podophyllotoxin ; 2.2.4 Synthesis of Puupehenol and Related Compounds; 2.2.5 Synthesis of (2212;)-Talaumidin ; 2.2.6 Total Synthesis of (±)-Schefferine ; 2.3 TOTAL SYNTHESIS INVOLVING INTRAMOLECULAR FC ALKYLATIONS; 2.3.1 C-C Bond Formation Leading to Homocyclic Rings ; 2.3.2 C-C Bond Formation Leading to Oxygen-Containing Rings ; 2.3.3 C-C Bond Formation Leading to Nitrogen-Containing Rings ; 2.4 TOTAL SYNTHESIS THROUGH TANDEM AND CASCADE PROCESSES INVOLVING FC REACTIONS 327 $a2.4.1 C-C Bond Formation Leading to Homocyclic Rings 2.4.2 C-C Bond Formation Leading to Oxygen-Containing Rings ; 2.4.3 C-C Bond Formation Leading to Nitrogen-Containing Rings ; 2.5 TOTAL SYNTHESIS INVOLVING ipso-FC REACTIONS ; 2.5.1 Synthesis of (S)-(2212;)-Xylopinine ; 2.5.2 Synthesis of Garcibracteatone; 2.6 SUMMARY AND OUTLOOK; 2.7 ACKNOWLEDGMENT; ABBREVIATIONS ; REFERENCES; CHAPTER 3 CATALYTIC FRIEDEL-CRAFTS ACYLATION REACTIONS ; 3.1 INTRODUCTION AND HISTORICAL BACKGROUND; 3.2 CATALYTIC HOMOGENEOUS ACYLATIONS; 3.2.1 Metal Halides 327 $a3.2.2 Perfluoroalkanoic Acids, Perfluorosulfonic Acids, and Their (Metal) Derivatives 3.2.3 Miscellaneous; 3.3 CATALYTIC HETEROGENEOUS ACYLATIONS; 3.3.1 Zeolites; 3.3.2 Clays; 3.3.3 Metal Oxides; 3.3.4 Acid-Treated Metal Oxides ; 3.3.5 Heteropoly Acids (HPAs); 3.3.6 Nafion; 3.3.7 Miscellaneous; 3.4 DIRECT PHENOL ACYLATION; 3.5 SUMMARY AND OUTLOOK; ABBREVIATIONS ; REFERENCES ; CHAPTER 4 THE USE OF QUANTUM CHEMISTRY FOR MECHANISTIC ANALYSES OF SEAr REACTIONS ; 4.1 INTRODUCTION; 4.1.1 Historical Overview of Early Quantum Chemistry Work 327 $a4.1.2 Current Mechanistic Understanding Based on Kinetic and Spectroscopic Studies 4.2 THE SEAr MECHANISM: QUANTUM CHEMICAL CHARACTERIZATION IN GAS PHASE AND SOLUTION; 4.2.1 Nitration and Nitrosation; 4.2.2 Halogenation; 4.2.3 Sulfonation; 4.2.4 Friedel-Crafts Alkylations and Acylations; 4.3 PREDICTION OF RELATIVE REACTIVITY AND REGIOSELECTIVITY BASED ON QUANTUM CHEMICAL DESCRIPTORS; 4.4 QUANTUM CHEMICAL REACTIVITY PREDICTION BASED ON MODELING OF TRANSITION STATES AND INTERMEDIATES; 4.4.1 Transition State Modeling; 4.4.2 The Reaction Intermediate or Sigma-Complex Approach 327 $a4.5 SUMMARY AND CONCLUSIONS 606 $aAromatic compounds 606 $aChemistry, Organic 615 0$aAromatic compounds. 615 0$aChemistry, Organic. 676 $a547/.61 702 $aMortier$b Jacques 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910827921703321 996 $aArene chemistry$94085476 997 $aUNINA