{"product_id":"stereoselective-organocatalysis-9781118203538","title":"Stereoselective Organocatalysis","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003e\u003cp\u003e\u003cb\u003eSets forth an important group of environmentally friendly organic reactions\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eWith contributions from leading international experts in organic synthesis, this book presents all the most important methodologies for stereoselective organocatalysis, fully examining both the activation mode as well as the type of bond formed. Clear explanations guide researchers through all the most important methods used to form key chemical bonds, including carbon-carbon (C?C), carbon-nitrogen (C?N), and carbon-halogen (C?X) bonds. Moreover, readers will discover how the use of non-metallic catalysts facilitates a broad range of important reactions that are environmentally friendly and fully meet the standards of green chemistry.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eStereoselective Organocatalysis\u003c\/i\u003e begins with an historical overview and a review of activation modes in asymmetric organocatalysis. The next group of chapters is organized by bond type, making it easy to find bonds according to their applications. The\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTrade Review\u003c\/b\u003e\u003cbr\u003e\u003c\/p\u003e\u003cp\u003e“The book is nicely structured and the chapters are extensively supplemented by references, offering the reader a practical overview of the field of asymmetric organocatalysis . . . Congratulations to the editor and to all the authors for this nice piece of work.”  (\u003ci\u003eAngew. Chem. Int. Ed\u003c\/i\u003e, 1 October 2014)\u003c\/p\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cp\u003ePREFACE vii\u003c\/p\u003e \u003cp\u003eCONTRIBUTORS ix\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1. INTRODUCTION: A HISTORICAL POINT OF VIEW 1\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eRamon Rios and Xavier Companyó\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2. ACTIVATION MODES IN ASYMMETRIC ORGANOCATALYSIS 11\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eAlbert Moyano\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3. C–C BOND FORMATION BY ALDOL REACTION 81\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eDorota Gryko and Dominika Walaszek\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4. EXAMPLES OF METAL-FREE DIRECT CATALYTIC ASYMMETRIC MANNICH-TYPE REACTIONS USING AMINOCATALYSIS 129\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eArmando Córdova\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5. C–C BOND FORMATION BY MICHAEL REACTION 147\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eYong Zhang and Wei Wang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6. C–C BOND FORMATION BY DIELS–ALDER AND OTHER PERICYCLIC REACTIONS 205\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJohan Franzén\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7. N-HETEROCYCLIC CARBENE-CATALYZED C–C BOND FORMATION 231\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eXiang-Yu Chen and Song Ye\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8. a-ALKYLATION OF CARBONYL COMPOUNDS 267\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eMarek Remeš and Jan Veselý\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e9. OTHER REACTIONS FOR C–C BOND FORMATION 313\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eYi-Xia Jia and Tiexin Zhang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e10. CASCADE REACTIONS FORMING C–C BONDS 351\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eRamon Rios, Jorge Esteban, and Xavier Companyó\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e11. ORGANOCATALYTIC C–N BOND FORMATION 381\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eAitor Landa, Rosa López, Antonia Mielgo, Mikel Oiarbide, and Claudio Palomo\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e12. C–O BOND FORMATION 433\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJosé Alemán and Mariola Tortosa\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e13. CARBON–HALOGEN BOND FORMATION 465\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eStacey E. Brenner-Moyer\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e14. C–OTHER ATOM BOND FORMATION (S, SE, B) 493\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eGiorgio Della Sala and Alessandra Lattanzi\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e15. ENANTIOSELECTIVE ORGANOCATALYTIC REDUCTIONS 529\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eMaurizio Benaglia, Martina Bonsignore, and Andrea Genoni\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e16. CASCADE REACTIONS FORMING BOTH C–C BOND AND C–HETEROATOM BOND 559\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eDamien Bonne, Thierry Constantieux, Yoann Coquerel, and Jean Rodriguez\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e17. ORGANOCATALYSIS IN THE SYNTHESIS OF NATURAL PRODUCTS 587\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eYongcheng Ying and Xuefeng Jiang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eINDEX 629\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49406840766807,"sku":"9781118203538","price":155.8,"currency_code":"GBP","in_stock":false}],"url":"https:\/\/bookcurl.com\/products\/stereoselective-organocatalysis-9781118203538","provider":"Book Curl","version":"1.0","type":"link"}