{"product_id":"name-reactions-in-heterocyclic-chemistry-hardback-9780471302155","title":"Name Reactions in Heterocyclic Chemistry (Hardback) 9780471302155","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eName Reactions in Heterocyclic Chemistry\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"4\"\u003eJie Jack Li (Edited by), JJ Li (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780471302155, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 2 November 2004\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e592 pages\u003cbr\u003e23.6 x 19.8 x 3.6 cm, 1.179 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cem\u003e\u003cfont size=\"3\"\u003e\"...is not only an indispensable resource for senior undergraduate and graduate students....but also a good reference for all chemists interested in the chemistry of heterocyclic compounds…\" (\u003ci\u003eDrug Development and Industrial Pharmacy\u003c\/i\u003e, No. 10, 2005)  \u003cp\u003e\"...a major contribution to the field and is highly recommended.\" (\u003ci\u003eJournal of Medicinal Chemistry\u003c\/i\u003e, June 30, 2005)\u003c\/p\u003e\u003c\/font\u003e\u003c\/em\u003e\u003c\/p\u003e\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eCovers important name reactions relevant to heterocyclic chemistry  \u003cp\u003eThe 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 both the professional research chemist as well as the advanced student.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eName Reactions in Heterocyclic Chemistry\u003c\/i\u003e provides a one-stop repository for this important field of organic chemistry. The primary topics include three- and four-membered heterocycles, five-membered heterocycles including indoles, furans, thiophenes, and oxazoles, six-membered heterocycles including quinolines, isoquinolines, and pyrimidines, and other heterocycles.\u003c\/p\u003e \u003cp\u003eEach name reaction is summarized in seven sections:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eDescription\u003c\/li\u003e \u003cli\u003eHistorical perspective\u003c\/li\u003e \u003cli\u003eMechanism\u003c\/li\u003e \u003cli\u003eVariations and improvements\u003c\/li\u003e \u003cli\u003eSynthetic utility\u003c\/li\u003e \u003cli\u003eExperimental\u003c\/li\u003e \u003cli\u003eReferences\u003c\/li\u003e \u003c\/ul\u003e Authored by a team of world-renowned contributors - some of whom have discovered the very reactions they describe - \u003ci\u003eName Reactions in Heterocyclic Chemistry\u003c\/i\u003e represents a state-of-the-art resource for students and researchers alike.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003eForeword x\u003c\/p\u003e \u003cp\u003ePreface xi\u003c\/p\u003e \u003cp\u003eAcronyms and abbreviations xiv\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 Epoxides and Aziridines 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 Corey-Chaykovsky reaction 2\u003c\/p\u003e \u003cp\u003e1.2 Darzens glycidic ester condensation 15\u003c\/p\u003e \u003cp\u003e1.3 Hoch-Campbell aziridine synthesis 22\u003c\/p\u003e \u003cp\u003e1.4 Jacobsen-Katsuki epoxidation 29\u003c\/p\u003e \u003cp\u003e1.5 Paterno-Büchi reaction 44\u003c\/p\u003e \u003cp\u003e1.6 Sharpless-Katsuki epoxidation 50\u003c\/p\u003e \u003cp\u003e1.7 Wenker aziridine synthesis 63\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePart 2 Five-Membered Heterocycles 69\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 2 \u003c\/b\u003e\u003cb\u003ePyrroles and Pyrrolidines 69\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Barton-Zard reaction 70\u003c\/p\u003e \u003cp\u003e2.2 Knorr and Paal-Knorr pyrrole syntheses 79\u003c\/p\u003e \u003cp\u003e2.3 Hofmann-Löffler-Freytag reaguo 90\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 3 Indoles 99\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Bartoli indole synthesis 100\u003c\/p\u003e \u003cp\u003e3.2 Batcho-Leimgruber indole synthesis 104\u003c\/p\u003e \u003cp\u003e3.3 Bucherer carbazole synthesis 110\u003c\/p\u003e \u003cp\u003e3.4 Fischer indole synthesis 116\u003c\/p\u003e \u003cp\u003e3.5 Gassman indole synthesis 128\u003c\/p\u003e \u003cp\u003e3.6 Graebe-Ullman carbazole synthesis 132\u003c\/p\u003e \u003cp\u003e3.7 Hegedus indole synthesis 135\u003c\/p\u003e \u003cp\u003e3.8 Madelung indole synthesis 140\u003c\/p\u003e \u003cp\u003e3.9 Nenitzescu indole synthesis 145\u003c\/p\u003e \u003cp\u003e3.10 Reissert indole synthesis 154\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 4 Furans\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Feist-Bénary furan synthesis 160\u003c\/p\u003e \u003cp\u003e4.2 Paal-Knorr furan synthesis 168\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 5 Thiophenes 183\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Fiesselmann thiophene synthesis 184\u003c\/p\u003e \u003cp\u003e5.2 Gewald aminothiophene synthesis 193\u003c\/p\u003e \u003cp\u003e5.3 Hinsberg synthesis of thiophene derivatives 199\u003c\/p\u003e \u003cp\u003e5.4 Paal thiophene synthesis 207\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 6 Oxazoles and Isoxazoles 219\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Claisen isoxazole synthesis 220\u003c\/p\u003e \u003cp\u003e6.2 Cornforth rearrangement 225\u003c\/p\u003e \u003cp\u003e6.3 Erlenmeyer-Plöchl azlactone synthesis 229\u003c\/p\u003e \u003cp\u003e6.4 Fischer oxazole synthesis 234\u003c\/p\u003e \u003cp\u003e6.5 Meyers oxazoline method 237\u003c\/p\u003e \u003cp\u003e6.6 Robinson-Gabriel synthesis 249\u003c\/p\u003e \u003cp\u003e6.7 van Leusen oxazole Synthesis 254\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 7 Other Five-Membered Heterocycles 261\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 Auwers flavone synthesis 262\u003c\/p\u003e \u003cp\u003e7.2 Bucherer-Bergs reaction 266\u003c\/p\u003e \u003cp\u003e7.3 Cook-Heilbron 5-amino-thiazole synthesis 275\u003c\/p\u003e \u003cp\u003e7.4 Hurd-Mori 1,2,3-thiadiazole synthesis 284\u003c\/p\u003e \u003cp\u003e7.5 Knorr pyrazole synthesis 392\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePart 3 Six-Membered Heterocycles 301\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 8 \u003c\/b\u003e\u003cb\u003ePyridines 302\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8.1 Preparation via condensation reactions 303\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1.1 Hantzsch (dihydro)-pyridine synthesis 304\u003c\/p\u003e \u003cp\u003e8.1.1.1 Description 304\u003c\/p\u003e \u003cp\u003e8.1.1.2 Historical perspective 304\u003c\/p\u003e \u003cp\u003e8.1.1.3 Mechanism 305\u003c\/p\u003e \u003cp\u003e8.1.1.4 Variations 307\u003c\/p\u003e \u003cp\u003e8.1.1.4.1 Guareschi-Thorpe pyridine synthesis 307\u003c\/p\u003e \u003cp\u003e8.1.1.4.2 Chichibabin (Tschitschibabin) pyridine synthesis 308\u003c\/p\u003e \u003cp\u003e8.1.1.4.3 Bohlmann-Rahtz pyridine synthesis 309\u003c\/p\u003e \u003cp\u003e8.1.1.4.4 Kröhnke pyridine synthesis 311\u003c\/p\u003e \u003cp\u003e8.1.1.4.5 Petrenko-Kritschenko piperidone synthesis 313\u003c\/p\u003e \u003cp\u003e8.1.1.5 Improvement or modifications 314\u003c\/p\u003e \u003cp\u003e8.1.1.6 Experimental 320\u003c\/p\u003e \u003cp\u003e8.1.1.6.1 Three-component coupling 320\u003c\/p\u003e \u003cp\u003e8.1.1.6.2 Two-component coupling 320\u003c\/p\u003e \u003cp\u003e8.1.1.7 References 321\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8.2 Preparation via cycloaddition reactions \u003c\/b\u003e\u003cb\u003e323\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.2.1 Boger reaction 323\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8.3 \u003c\/b\u003e\u003cb\u003ePreparation via rearrangement reactions\u003c\/b\u003e\u003cb\u003e 340\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.3.1 Boekelheide reaction 340\u003c\/p\u003e \u003cp\u003e8.3.2 Ciamician-Dennstedt rearrangement 350\u003c\/p\u003e \u003cp\u003e8.4 Zincke reaction 355\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 9 Quinolines and Isoquinolines \u003c\/b\u003e\u003cb\u003e375\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e9.1 Bischler-Napieralski reaction 376\u003c\/p\u003e \u003cp\u003e9.2 Camps quinoline synthesis 386\u003c\/p\u003e \u003cp\u003e9.3 Combes quinoline synthesis 390\u003c\/p\u003e \u003cp\u003e9.4 Conrad-Limpach reaction 398\u003c\/p\u003e \u003cp\u003e9.5 Doebner quinoline synthesis 407\u003c\/p\u003e \u003cp\u003e9.6 Friedländer synthesis 411\u003c\/p\u003e \u003cp\u003e9.7 Gabriel-Colman rearrangement 416\u003c\/p\u003e \u003cp\u003e9.8 Gould-Jacobs reaction 423\u003c\/p\u003e \u003cp\u003e9.9 Knorr quinoline synthesis 437\u003c\/p\u003e \u003cp\u003e9.10 Meth-Cohn quinoline synthesis 443\u003c\/p\u003e \u003cp\u003e9.11 Pfitzinger quinoline synthesis 451\u003c\/p\u003e \u003cp\u003e9.12 Pictet-Gams isoquinoline synthesis 457\u003c\/p\u003e \u003cp\u003e9.13 Pictet-Hubert reaction 465\u003c\/p\u003e \u003cp\u003e9.14 Pictet-Spengler isoquinoline synthesis 469\u003c\/p\u003e \u003cp\u003e9.15 Pomeranz-Fritsch reaction 480\u003c\/p\u003e \u003cp\u003e9.16 Riehm quinoline synthesis 487\u003c\/p\u003e \u003cp\u003e9.17 Skraup\/Doebner-von Miller reaction 488\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 10 Other Six-Membered Heterocycles\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e10.1 Algar-Flynn-Oyamada reaction 496\u003c\/p\u003e \u003cp\u003e10.2 Beirut reaction 504\u003c\/p\u003e \u003cp\u003e10.3 Biginelli reaction 509\u003c\/p\u003e \u003cp\u003e10.4 Kostanecki-Robinson reaction 521\u003c\/p\u003e \u003cp\u003e10.5 Pinner pyrimidine synthesis 536\u003c\/p\u003e \u003cp\u003e10.6 von Richter cinnoline reaction 540\u003c\/p\u003e \u003cp\u003eSubject Index 545\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-Interscience","offers":[{"title":"Brand New","offer_id":52286440243480,"sku":"9780471302155","price":144.55,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780471302155.jpg?v=1781551939","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/name-reactions-in-heterocyclic-chemistry-hardback-9780471302155","provider":"Freshly Printed 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