LEADER 00905nam0 2200265 450 001 000001081 005 20050630115300.0 010 $a88-13-18331-3 100 $a--------d1993----km-y0itay50------ba 101 $aita 102 $aIT 200 1 $a<>capacità contributiva$fFrancesco Moschetti, Gianfranco Lorenzon... [et al.]$ga cura di Francesco Moschetti 210 $aPadova$cCEDAM$d1993 215 $aVIII, 158 p.$d24 cm 300 $aEstratto dal: Trattato di diritto tributario, vol. 1, I/ diretto da Andrea Amatucci 610 1 $aCapacità contributiva 676 $a343.4504 701 1$aMoschetti,$bFrancesco$0229146 701 1$aLorenzon,$bGianfranco$0629980 701 1$aSchiavolin,$bRoberto$0233837 801 0$aIT $bUNIPARTHENOPE $gRICA $2UNIMARC 912 $a000001081 951 $cNAVA1$a343-C/15$b33001$d20000322 996 $aCapacità contributiva$91223266 997 $aUNIPARTHENOPE LEADER 01217nam0 22003013i 450 001 SUN0100710 005 20150202032600.571 010 $d0.00 100 $a20150129d1959 |0itac50 ba 101 $aita 102 $aIT 105 $a|||| ||||| 200 1 $aAdenauer e la nuova Germania$fEdgar Alexander$gprefazione Luigi Sturzo$gtraduzione Cordelia Gundolf 205 $aNapoli : Politica Popolare$b1959 210 $d475 p., [2] carte di tav. : ill. ; 22 cm 215 $aBiblioteca Lauria. 606 $aAdenauer Konrad Herman Josef$2SG$3SUNC030525 620 $dNapoli$3SUNL000005 700 1$aAlexander$b, Edgar$3SUNV078856$0396123 702 1$aSturzo$b, Luigi$3SUNV004575 702 1$aGundolf$b, Cordelia$3SUNV078857$4730 712 $aEdizioni politica popolare$3SUNV009592$4650 801 $aIT$bSOL$c20181109$gRICA 912 $aSUN0100710 950 $aUFFICIO DI BIBLIOTECA DEL DIPARTIMENTO DI GIURISPRUDENZA$d00 CONS BL.900M.129 $e00 BL 4428 995 $aUFFICIO DI BIBLIOTECA DEL DIPARTIMENTO DI GIURISPRUDENZA$gBL$h4428$kCONS BL.900M.129$oc$qa 996 $aAdenauer und das neue Deutschland$940943 997 $aUNICAMPANIA LEADER 05338nam 22006494a 450 001 9910830429203321 005 20230617031007.0 010 $a1-280-27303-8 010 $a9786610273034 010 $a0-470-35202-7 010 $a0-471-70414-8 010 $a0-471-70415-6 035 $a(CKB)1000000000018994 035 $a(EBL)221302 035 $a(OCoLC)123417691 035 $a(SSID)ssj0000207813 035 $a(PQKBManifestationID)11194285 035 $a(PQKBTitleCode)TC0000207813 035 $a(PQKBWorkID)10238115 035 $a(PQKB)11120009 035 $a(MiAaPQ)EBC221302 035 $a(EXLCZ)991000000000018994 100 $a20040518d2005 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aName reactions in heterocyclic chemistry$b[electronic resource] /$fedited by Jie-Jack Li 210 $aHoboken, N.J. $cWiley-Interscience$dc2005 215 $a1 online resource (579 p.) 225 1 $aComprehensive Name Reactions ;$vv.3 300 $aDescription based upon print version of record. 311 $a0-471-30215-5 320 $aIncludes bibliographical references and index. 327 $aName Reactions in Heterocyclic Chemistry; Table of Contents; Foreword; Preface; Acronyms and abbreviations; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Epoxides and Aziridines; 1.1 Corey-Chaykovsky reaction; 1.2 Darzens glycidic ester condensation; 1.3 Hoch-Campbell aziridine synthesis; 1.4 Jacobsen-Katsuki epoxidation; 1.5 Paterno-Buchi reaction; 1.6 Sharpless-Katsuki epoxidation; 1.7 Wenker aziridine synthesis; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Barton-Zard reaction; 2.2 Knorr and Paal-Knorr pyrrole syntheses 327 $a2.3 Hofmann-Loffler-Freytag reactionChapter 3 Indoles; 3.1 Bartoli indole synthesis; 3.2 Batcho-Leimgruber indole synthesis; 3.3 Bucherer carbazole synthesis; 3.4 Fischer indole synthesis; 3.5 Gassman indole synthesis; 3.6 Graebe-Ullman carbazole synthesis; 3.7 Hegedus indole synthesis; 3.8 Madelung indole synthesis; 3.9 Nenitzescu indole synthesis; 3.10 Reissert indole synthesis; Chapter 4 Furans; 4.1 Feist-Benary furan synthesis; 4.2 Paal-Knorr furan synthesis; Chapter 5 Thiophenes; 5.1 Fiesselmann thiophene synthesis; 5.2 Gewald aminothiophene synthesis 327 $a5.3 Hinsberg synthesis of thiophene derivatives5.4 Paal thiophene synthesis; Chapter 6 Oxazoles and Isoxazoles; 6.1 Claisen isoxazole synthesis; 6.2 Cornforth rearrangement; 6.3 Erlenmeyer-Plochl azlactone synthesis; 6.4 Fischer oxazole synthesis; 6.5 Meyers oxazoline method; 6.6 Robinson-Gabriel synthesis; 6.7 van Leusen oxazole Synthesis; Chapter 7 Other Five-Membered Heterocycles; 7.1 Auwers flavone synthesis; 7.2 Bucherer-Bergs reaction; 7.3 Cook-Heilbron 5-amino-thiazole synthesis; 7.4 Hurd-Mori 1,2,3-thiadiazole synthesis; 7.5 Knorr pyrazole synthesis; PART 3 SIX-MEMBERED HETEROCYCLES 327 $aChapter 8 Pyridines8.1 Preparation via condensation reactions; 8.1.1 Hantzsch (dihydro)-pyridine synthesis; 8.1.1.1 Description; 8.1.1.2 Historical perspective; 8.1.1.3 Mechanism; 8.1.1.4 Variations; 8.1.1.4.1 Guareschi-Thorpe pyridine synthesis; 8.1.1.4.2 Chichibabin (Tschitschibabin) pyridine synthesis; 8.1.1.4.3 Bohlmann-Rahtz pyridine synthesis; 8.1.1.4.4 Krohnke pyridine synthesis; 8.1.1.4.5 Petrenko-Kritschenko piperidone synthesis; 8.1.1.5 Improvements or modifications; 8.1.1.6 Experimental; 8.1.1.6.1 Three-component coupling; 8.1.1.6.2 Two-component coupling; 8.1.1.7 References 327 $a8.2 Preparation via cycloaddition reactions8.2.1 Boger reaction; 8.3 Preparation via rearrangement reactions; 8.3.1 Boekelheide reaction; 8.3.2 Ciamician-Dennstedt rearrangement; 8.4 Zincke reaction; Chapter 9 Quinolines and Isoquinolines; 9.1 Bischler-Napieralski reaction; 9.2 Camps quinoline synthesis; 9.3 Combes quinoline synthesis; 9.4 Conrad-Limpach reaction; 9.5 Doebner quinoline synthesis; 9.6 Friedlander synthesis; 9.7 Gabriel-Colman rearrangement; 9.8 Gould-Jacobs reaction; 9.9 Knorr quinoline synthesis; 9.10 Meth-Cohn quinoline synthesis; 9.11 Pfitzinger quinoline synthesis 327 $a9.12 Pictet-Gams isoquinoline synthesis 330 $aCovers important name reactions relevant to heterocyclic chemistry The field of heterocyclic chemistry has long presented a special challenge for chemists. Because of the enormous amount and variety of information, it is often a difficult topic to cover for undergraduate and graduate chemistry students, even in simplified form. Yet the chemistry of heterocyclic compounds and methods for their synthesis form the bedrock of modern medicinal chemical and pharmaceutical research. Thus there is a great need for high quality, up-to-date, and authoritative books on heterocyclic synthesis helpful to 410 0$aComprehensive Name Reactions 606 $aHeterocyclic chemistry 606 $aChemical reactions 615 0$aHeterocyclic chemistry. 615 0$aChemical reactions. 676 $a547.59 676 $a547.590459 701 $aLi$b Jie Jack$0440094 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830429203321 996 $aName reactions in heterocyclic chemistry$93995394 997 $aUNINA