{"product_id":"organic-reactions-volume-100-hardback-9781119456667","title":"Organic Reactions, Volume 100 (Hardback) 9781119456667","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eOrganic Reactions, Volume 100\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\"\u003eScott E. Denmark (Editor-in-chief), SE Denmark (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9781119456667, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 2 January 2020\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e1136 pages\u003cbr\u003e23.1 x 15.5 x 4.6 cm, 1.406 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eWritten by a \"who is who\" of leading organic chemists, this anniversary volume represent the Organic Reactions editors' choice of the most important, ground-breaking and versatile reactions in current organic synthesis. The 15 reaction types selected for this volume include reactions for carbon-carbon bond formation, cross-coupling reactions, hydro- and halofunctionalizations, among many others.\u003cbr\u003e In line with the successful recipe of the series, each chapter is focused on a single reaction, discussing its mechanism and stereochemistry, scope and limitations, applications to synthesis, comparison with other methods, and experimental procedures. Each chapter concludes with a tabular survey of selected key application examples, complete with reported reaction conditions and yields, to serve as a quick reference guide for synthesis planning.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003e1. The Negishi Cross-Coupling Reaction 1\u003cbr\u003e \u003ci\u003eColin Diner and Michael G. Organ\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e2. Generation and Trapping of Functionalized Aryl- and Heteroarylmagnesium and -Zinc Compounds 63\u003cbr\u003e \u003ci\u003eFerdinand H. Lutter, Maximilian S. Hofmayer, Jeffrey M. Hammann, Vladimir Malakhov, and Paul Knochel\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e3. Copper-Catalyzed, Enantioselective Hydrofunctionalization of Alkenes 121\u003cbr\u003e \u003ci\u003eHaoxuan Wang and Stephen L. Buchwald\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e4. The Catalytic, Enantioselective Favorskii Reaction: in Situ Formation of Metal Alkynylides and Their Additions to Aldehydes 207\u003cbr\u003e \u003ci\u003eYeshua Sempere and Erick M. Carreira\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e5. Enantioselective Lithiation–Substitution of Nitrogen-Containing Heterocycles 255\u003cbr\u003e \u003ci\u003eKevin Kasten, Nico Seling, and Peter O’Brien\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e6. Catalytic, Enantioselective, Transfer Hydrogenation 329\u003cbr\u003e \u003ci\u003eMasahiro Yoshimura and Masato Kitamura\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e7. Hydrofunctionalization of Alkenes by Hydrogen-Atom Transfer 383\u003cbr\u003e \u003ci\u003eRyan A. Shenvi, Jeishla L. M. Matos, and Samantha A. Green\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e8. Carbon–Carbon Bond Formation by Metallaphotoredox Catalysis 471\u003cbr\u003e \u003ci\u003eEric D. Nacsa and David W. C. MacMillan\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e9. Suzuki–Miyaura Cross-Coupling 547\u003cbr\u003e \u003ci\u003eAlexander B. Pagett and Guy C. Lloyd-Jones\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e10. \u003ci\u003eortho\u003c\/i\u003e-Directed C–H Alkylation of Substituted Benzenes 621\u003cbr\u003e \u003ci\u003eYusuke Ano and Naoto Chatani \u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e11. Catalytic, Enantioselective, C–H Functionalization to Form Carbon–Carbon Bonds 671\u003cbr\u003e \u003ci\u003eQing-Feng Wu, Gang Chen, Jian He, and Jin-Quan Yu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e12. Catalytic, Enantioselective Fluorination Reactions 749\u003cbr\u003e \u003ci\u003eRichard T. Thornbury and F. Dean Toste\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e13. Catalyst-Controlled Glycosylation 801\u003cbr\u003e \u003ci\u003eSamuel M. Levi and Eric N. Jacobsen\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e14. Palladium-Catalyzed Amination of Aryl Halides 853\u003cbr\u003e \u003ci\u003eJohn F. Hartwig, Kevin H. Shaughnessy, Shashank Shekhar, and Rebecca A. Green\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e15. Catalytic, Enantioselective, Copper–Boryl Additions to Alkenes 959\u003cbr\u003e \u003ci\u003eAmir H. Hoveyda, Ming Joo Koh, Kyunga Lee, and Jaehee Lee\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eCumulative Chapter Titles by Volume 1057\u003c\/p\u003e \u003cp\u003eAuthor Index, Volumes 1–100 1075\u003c\/p\u003e \u003cp\u003eChapter and Topic Index, Volumes 1–100 1083\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","offers":[{"title":"Brand New","offer_id":52428597920024,"sku":"9781119456667","price":226.99,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9781119456667.jpg?v=1784680846","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/organic-reactions-volume-100-hardback-9781119456667","provider":"Freshly Printed Books","version":"1.0","type":"link"}