LEADER 01216nam a2200325 i 4500 001 991001914639707536 005 20020503154907.0 008 981224s1968 it ||| | ita 035 $ab10290564-39ule_inst 035 $aEXGIL93592$9ExL 040 $aDip.to Filol. Ling. e Lett.$bita 082 0 $a891.7 100 1 $aTynjanov, Jurij Nikolaevic$0456399 245 10$aAvanguardia e tradizione /$cJurij Tynjanov ; introduzione di Viktor Sklovskij 260 $aBari :$bDedalo libri,$c[c1968] 300 $a352 p. ;$c21 cm. 440 3$aLa scienza nuova ;$v4 500 $aTrad. S. Leone 500 $aA cura di M. Marzaduri 650 4$aLetteratura russa$xSaggi 700 1 $aMarzaduri, Mario 700 1 $aLeone, Sergio 740 0 $aArhaisty i novatory 907 $a.b10290564$b21-09-06$c27-06-02 912 $a991001914639707536 945 $aLE008 L. Glott. 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Mondadori,$c1991 (c1983) 300 $aLIX, 223 p. ;$c20 cm 490 0 $aOscar classici greci e latini ;$v10 500 $aTesto greco con traduzione italiana a fronte 700 1 $aAlbini, Umberto 700 1 $aFaggi, Vico 700 1 $aMatteuzzi, Maurizia 740 3 $aLe Trachinie 907 $a.b10929551$b23-02-17$c28-06-02 912 $a991001899719707536 945 $aLE007 880.1 Sophocles 1991-03$g1$i2015000110275$lle007$o-$pE0.00$q-$rl$s- $t0$u19$v6$w19$x0$y.i11034440$z28-06-02 996 $aAiace$9920050 997 $aUNISALENTO 998 $ale007$b01-01-94$cm$da $e-$fita$git $h0$i1 LEADER 05393nam 2200757Ia 450 001 9910817213403321 005 20200520144314.0 010 $a9786613282705 010 $a9781283282703 010 $a1283282704 010 $a9781118092842 010 $a1118092848 010 $a9781118092859 010 $a1118092856 010 $a9781118092828 010 $a1118092821 035 $a(CKB)3270000000000220 035 $a(EBL)693162 035 $a(OCoLC)761319808 035 $a(SSID)ssj0000582849 035 $a(PQKBManifestationID)11347535 035 $a(PQKBTitleCode)TC0000582849 035 $a(PQKBWorkID)10564280 035 $a(PQKB)10330033 035 $a(MiAaPQ)EBC693162 035 $a(Au-PeEL)EBL693162 035 $a(CaPaEBR)ebr10560664 035 $a(CaONFJC)MIL328270 035 $a(Perlego)1013104 035 $a(EXLCZ)993270000000000220 100 $a20120202d2011 uy 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt 182 $cc 183 $acr 200 00$aName reactions in heterocyclic chemistry II /$fedited by Jie Jack Li ; foreword by E.J. Corey 205 $a1st ed. 210 $aHoboken, N.J. $cWiley$dc2011 215 $a1 online resource (706 p.) 225 1 $aWiley series on comprehensive name reactions ;$vv. 6 300 $aDescription based upon print version of record. 311 08$a9780470085080 311 08$a0470085088 320 $aIncludes bibliographical references and index. 327 $aName Reactions in Heterocyclic Chemistry II; Contents; Foreword; Preface; Contributing Authors; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Aziridines and Epoxides; 1.1 Blum Aziridine Synthesis; 1.2 Gabriel-Heine Aziridine Isomerization; 1.3 Shi Epoxidation; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Clauson-Kass Pyrrole Synthesis; 2.2 Houben-Hoesch Acylation of Pyrroles; 2.3 Overman Pyrrolidine Synthesis; 2.4 Trofimov Synthesis of Pyrroles; Chapter 3 Indoles; 3.1 Bischler-Mo?hlau Indole Synthesis; 3.2 Borsche-Drechsel Cyclization 327 $a3.3 Buchwald-Hartwig Indole Synthesis 3.4 Cadogan-Sundberg Indole Synthesis; 3.5 Fukuyama Indole Synthesis; 3.6 Gassman Oxindole Synthesis; 3.7 Larock Indole Synthesis; 3.8 Matinet Dioxindole Reaction; 3.9 Mori-Ban Indole Synthesis; 3.10 Sandmeyer Isatin Synthesis; 3.11 Sommelet-Hauser Rearrangement; 3.12 Stolle? Oxindole Synthesis; Chapter 4 Furans and Oxazoles; 4.1 Nierenstein Reaction; 4.2 Davidson Oxazole Synthesis; 4.3 Fischer Oxazole Synthesis; 4.4 Japp Oxazole Synthesis; 4.5 Scho?llkopf Oxazole Synthesis; Chapter 5 Other Five-Membered Heterocycles; 5.1 Bamberger Imidazole Cleavage 327 $a5.2 Dimroth Triazole Synthesis 5.3 Finnegan Tetrazole Synthesis; 5.4 Hantzsch Thiazole Synthesis; 5.5 Huisgen Tetrazole Rearrangement; 5.6 Knorr Pyrazole Synthesis; 5.7 Pechmann Pyrazole Synthesis; PART 3 SIX-MEMBERED HETEROCYCLES; Chapter 6 Pyridines; 6.1 Baeyer Pyridine Synthesis; 6.2 Katrizky Pyridine Synthesis; Chapter 7 Quinolines and Isoquinolines; 7.1 Betti Reaction; 7.2 Bernthsen Acridine Synthesis; 7.3 Lehmstedt- Ta?na?sescu Reaction; 7.4 Niementowski Quinoline Synthesis; 7.5 Povarov Reaction; Chapter 8 Six-Membered Heterocycles; 8.1 Balaban-Nenitzescu-Praill Reaction 327 $a8.2 Borsche Cinnoline Synthesis 8.3 Gutknecht Pyrazine Synthesis; 8.4 Niementowski Quinazoline Synthesis; 8.5 Pechmann Coumarin Synthesis; 8.6 Robinson-Scho?pf Condensation; 8.7 Simonis Chromone Cyclization; 8.8 Wesseley-Moser Rearrangement; 8.9 Widman-Stoermer Cinnoline Synthesis; 8.10 Wichterle Reaction; Chapter 9 Miscellaneous Name Reactions; 9.1 ANRORC Mechanism; 9.2 Boulton-Katritzky Rearrangement; 9.3 Chichibabin Amination Reaction; 9.4 Dimroth Rearrangement; 9.5 Hantzsch Synthesis; 9.6 Ortoleva-King Reaction; Appendixes 327 $aAppendix 1, Table of Contents for Volume 1 : Name Reactions in Heterocyclic Chemistry Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations; Appendix 3, Table of Contents for Volume 3: Name Reactions for Homologations-I; Appendix 4, Table of Contents for Volume 4: Name Reactions for Homologations-II; Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations; Subject Index 330 $aThe up-to-DATE guide to name reactions in heterocyclic chemistry Name Reactions in Heterocyclic Chemistry II presents a comprehensive treatise on name reactions in heterocyclic chemistry, one of the most exciting-and important-fields within organic chemistry today. The book not only covers fresh ground, but also provides extensive information on new and/or expanded reactions in: Three- and four-membered heterocycles Five-membered heterocycles (pyrroles and pyrrolidines, indoles, furans, thiophenes, and oxazoles) Six-membered heterocycles, including pyrid 410 0$aComprehensive name reactions ;$vv. 6. 606 $aHeterocyclic chemistry 606 $aChemical reactions 615 0$aHeterocyclic chemistry. 615 0$aChemical reactions. 676 $a547.2 701 $aLi$b Jie Jack$0440094 701 $aCorey$b E. J$020674 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910817213403321 996 $aName reactions in heterocyclic chemistry II$93970620 997 $aUNINA