{"product_id":"name-reactions-in-heterocyclic-chemistry-ii-9780470085080","title":"Name Reactions in Heterocyclic Chemistry II","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eCo-authored by Nobel Laureatte, E.J. Corey, this book builds on the first volume on this topic by presenting a comprehensive treatise on name reactions in heterocyclic chemistry.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cp\u003eForeword viii\u003c\/p\u003e \u003cp\u003ePreface ix\u003c\/p\u003e \u003cp\u003eContributing Authors xi\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePart 1 Three- and Four-Membered Heterocycles 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 1 Aziridines and Epoxides 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 Blum Aziridine Synthesis 2\u003c\/p\u003e \u003cp\u003e1.2 Gabriel-Heine Aziridine Isomerization 11\u003c\/p\u003e \u003cp\u003e1.3 Shi Epoxidation 21\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePart 2 Five-Membered Heterocycles 41\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 2 Pyrroles and Pyrrolidines 41\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Clauson-Kass Pyrrole Synthesis 42\u003c\/p\u003e \u003cp\u003e2.2 Houben-Hoesch Acylation of Pyrroles 53\u003c\/p\u003e \u003cp\u003e2.3 Overman Pyrrolidine Synthesis 60\u003c\/p\u003e \u003cp\u003e2.4 Trofimov Synthesis of Pyrroles 72\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 3 Indoles 83\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Bischler-Möhlau Indole Synthesis 84\u003c\/p\u003e \u003cp\u003e3.2 Borsche-Drechsel Cyclization 91\u003c\/p\u003e \u003cp\u003e3.3 Buchwald-Hartwig Indole Synthesis 102\u003c\/p\u003e \u003cp\u003e3 .4 Cadogan-Sundberg Indole Synthesis 112\u003c\/p\u003e \u003cp\u003e3.5 Fukuyama Indole Synthesis 125\u003c\/p\u003e \u003cp\u003e3.6 Gassman Oxindole Synthesis 133\u003c\/p\u003e \u003cp\u003e3.7 Larock Indole Synthesis 143\u003c\/p\u003e \u003cp\u003e3.8 Matinet Dioxindole Reaction 167\u003c\/p\u003e \u003cp\u003e3.9 Mori-Ban Indole Synthesis 175\u003c\/p\u003e \u003cp\u003e3.10 Sandmeyer Isatin Synthesis 187\u003c\/p\u003e \u003cp\u003e3.11 Sommelet-Hauser Rearrangement 197\u003c\/p\u003e \u003cp\u003e3.12 Stolle Oxindole Synthesis 207\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 4 Furans and Ox azoles 213\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Nierenstein Reaction 214\u003c\/p\u003e \u003cp\u003e4.2 Davidson Oxazole Synthesis 221\u003c\/p\u003e \u003cp\u003e4.3 Fischer Oxazole Synthesis 225\u003c\/p\u003e \u003cp\u003e4.4 Japp Oxazole Synthesis 233\u003c\/p\u003e \u003cp\u003e4.5 Schhllkopf Oxazole Synthesis 242\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 5 Other Five-Mem be red Heterocycles 259\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5. L Bamberger Imidazole Cleavage 260\u003c\/p\u003e \u003cp\u003e5.2 Dimroth Triazole Synthesis 269\u003c\/p\u003e \u003cp\u003e5.3 Finnegan Tetrazole Synthesis 278\u003c\/p\u003e \u003cp\u003e5.4 Hantzsch Thiazole Synthesis 299\u003c\/p\u003e \u003cp\u003e5.5 Huisgen Tetrazole Rearrangement 309\u003c\/p\u003e \u003cp\u003e5.6 Knorr Pyrazole Synthesis 317\u003c\/p\u003e \u003cp\u003e5.7 Pechmann Pyrazole Synthesis 327\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePart 3 Six-Membered Heterocycles 337\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 6 Pyridincs 337\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Baeyer Pyridine Synthesis 338\u003c\/p\u003e \u003cp\u003e6.2 Katrizky Pyridine Synthesis 347\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 7 Quinolines and Isoquinolines 351\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 Betti Reaction 352\u003c\/p\u003e \u003cp\u003e7.2 Bemthsen Acridine Synthesis 360\u003c\/p\u003e \u003cp\u003e7.3 Lehmstedt-Tanasescu Reaction 368\u003c\/p\u003e \u003cp\u003e7.4 Niementowski Quinoline Synthesis 376\u003c\/p\u003e \u003cp\u003e7.5 Povarov Reaction 385\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 8 Six-Membered Heterocycles 401\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1 Balaban-Nenitzescu-Praill Reaction 402\u003c\/p\u003e \u003cp\u003e8.2 Borsche Cinnoline Synthesis 420\u003c\/p\u003e \u003cp\u003e8.3 Gutknecht Pyrazine Synthesis 430\u003c\/p\u003e \u003cp\u003e8.4 Niementowski Quinazoline Synthesis 440\u003c\/p\u003e \u003cp\u003e8.5 Pechmann Coumarin Synthesis 454\u003c\/p\u003e \u003cp\u003e8.6 Robin son-Schöpf Condensation 470\u003c\/p\u003e \u003cp\u003e8.7 Simonis Chromone Cyclization 477\u003c\/p\u003e \u003cp\u003e8.8 Wesseley—Moser Rearrangement 487\u003c\/p\u003e \u003cp\u003e8.9 Widman-Stoermer Cinnoline Synthesis 493\u003c\/p\u003e \u003cp\u003e8.10 Wichterle Reaction 497\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 9 Miscellaneous Name Reactions 515\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e9.1 ANRORC Mechanism 516\u003c\/p\u003e \u003cp\u003e9.2 Boulton-Katritzky Rearrangement 527\u003c\/p\u003e \u003cp\u003e9.3 Chichibabin Animation Reaction 539\u003c\/p\u003e \u003cp\u003e9.4 Dimroth Rearrangement 554\u003c\/p\u003e \u003cp\u003e9.5 Hantzsch Synthesis 591\u003c\/p\u003e \u003cp\u003e9.6 Ortolcva-King Reaction 645\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAppendixes  \u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eAppendix 1, Table of Contents for Volume 1: Name Reactions in Heterocyclic Chemistry 651\u003c\/p\u003e \u003cp\u003eAppendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations 655\u003c\/p\u003e \u003cp\u003eAppendix 3, Table of Contents for Volume 3: Name Reactions for Hornolegations-I 657\u003c\/p\u003e \u003cp\u003eAppendix 4, Table of Contents for Volume 4; Name Reactions for Hornohgations-II 659\u003c\/p\u003e \u003cp\u003eAppendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations 661\u003c\/p\u003e \u003cp\u003eSubject Index 663\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49402281361751,"sku":"9780470085080","price":127.76,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9780470085080.jpg?v=1730479935","url":"https:\/\/bookcurl.com\/products\/name-reactions-in-heterocyclic-chemistry-ii-9780470085080","provider":"Book Curl","version":"1.0","type":"link"}