01097nam0 2200301 450 00000599420080404094653.088-141-0355-020051026d2003----km-y0itay50------baitaITy-------011yyAmicitiae pignusstudi in ricordo di Adriano Cavannaa cura di Antonio Padoa Schioppa, Gigliola di Renzo Villata, Gian Paolo MassettoMilanoGiuffrè20033 v. (X, 2408 p. compless.)24 cmPubblicazioni dell'Istituto di storia del diritto medievale e moderno00312001Pubblicazioni dell'Istituto di storia del diritto medievale e modernoCavanna,AdrianoPadoa-Schioppa,AntonioDi Renzo Villata,Maria GigliolaMassetto,Gian PaoloITUNIPARTHENOPE20051026RICAUNIMARC000005994B-006336782 (1)NAVA3B-006436782 (2)NAVA3B-006536782 (3)NAVA3Amicitiae pignus1104136UNIPARTHENOPE05227nam 2200673Ia 450 991013799850332120230725045336.01-283-28270-497866132827051-118-09284-81-118-09285-61-118-09282-1(CKB)3270000000000220(EBL)693162(OCoLC)761319808(SSID)ssj0000582849(PQKBManifestationID)11347535(PQKBTitleCode)TC0000582849(PQKBWorkID)10564280(PQKB)10330033(MiAaPQ)EBC693162(Au-PeEL)EBL693162(CaPaEBR)ebr10560664(CaONFJC)MIL328270(EXLCZ)99327000000000022020120202d2011 uy 0engurcn|||||||||txtccrName reactions in heterocyclic chemistry II[electronic resource] /edited by Jie Jack Li ; foreword by E.J. CoreyHoboken, N.J. Wileyc20111 online resource (706 p.)Wiley series on comprehensive name reactions ;v. 6Description based upon print version of record.0-470-08508-8 Includes bibliographical references and index.Name 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-Möhlau Indole Synthesis; 3.2 Borsche-Drechsel Cyclization3.3 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 Stollé 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 Schöllkopf Oxazole Synthesis; Chapter 5 Other Five-Membered Heterocycles; 5.1 Bamberger Imidazole Cleavage5.2 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- Tănăsescu Reaction; 7.4 Niementowski Quinoline Synthesis; 7.5 Povarov Reaction; Chapter 8 Six-Membered Heterocycles; 8.1 Balaban-Nenitzescu-Praill Reaction8.2 Borsche Cinnoline Synthesis 8.3 Gutknecht Pyrazine Synthesis; 8.4 Niementowski Quinazoline Synthesis; 8.5 Pechmann Coumarin Synthesis; 8.6 Robinson-Schöpf 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; AppendixesAppendix 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 IndexThe 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 pyridComprehensive name reactions ;v. 6.Heterocyclic chemistryChemical reactionsHeterocyclic chemistry.Chemical reactions.547.2Li Jie Jack440094Corey E. J20674MiAaPQMiAaPQMiAaPQBOOK9910137998503321Name reactions in heterocyclic chemistry II2085656UNINA