{"product_id":"the-chemistry-of-organocopper-compounds-set-9780470772966","title":"The Chemistry of Organocopper Compounds Set","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eCopper in organic synthesis has seen a tremendous development over the past ten years. This text represents the most comprehensive survey on the use of Copper and Cuprates in organic synthesis. The first time that the Patai Series touches on Copper compounds, it contains contributions by leading experts, and delivers the quality expected from the Patai Series.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e1. Theory of organocopper-mediated reactions (\u003ci\u003eEiichi Nakamura and Naohiko Yoshikai\u003c\/i\u003e).  \u003cp\u003e2. Structural organocopper chemistry (\u003ci\u003eGerard van Koten and Johann T. B. H. Jastrzebski\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e3. Thermochemistry of organocopper compounds (\u003ci\u003eJoel F. Liebman and Suzanne W. Slayden\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e4. NMR spectra of organocopper compounds (\u003ci\u003eTobias Gärtner and Ruth M. Gschwind\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e5. Photochemical transformations involving copper porphyrins and phthalocyanines (\u003ci\u003eNatalia N. Sergeeva and Mathias O. Senge\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e6. Electrochemistry of organocopper compounds (\u003ci\u003eJan S. Jaworski\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e7. Gas-phase chemistry of organocopper compounds (\u003ci\u003eAl Mokhtar Lamsabhi, Manuel Yáñez, Jean-Yves Salpin and Jeanine Tortajada\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e8. Biochemistry of organocopper compounds (\u003ci\u003eMartha E. Sosa-Torres, Juan Pablo Saucedo-Vázquez, Saul Gómez-Manzo and Peter M. H. Kroneck\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e9. \u003ci\u003eN\u003c\/i\u003e -Functionalized organocuprates (\u003ci\u003eR. Karl Dieter and Rhett T. Watson\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e10. Transmetalation reactions producing organocopper compounds (\u003ci\u003eChristopher J. Rosenker and Peter Wipf\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e11. Carbocupration of alkynes (\u003ci\u003eFabrice Chemla and Franck Ferreira\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e12. Oxidation of organocopper compounds (\u003ci\u003eSarah J. Aves and David R. Spring\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e13. Copper-mediated asymmetric allylic alkylations (\u003ci\u003eClaude Spino\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e14. Copper-catalyzed enantioselective conjugate addition (\u003ci\u003eDamien Polet and Alexandre Alexakis\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e15. Copper(I) hydride reagents and catalysts (\u003ci\u003eOlivier Riant\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e16. Silyl and stannyl derivatives of organocopper compounds (\u003ci\u003eFrancisco J. Pulido and Asunción Barbero\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e17. Copper-mediated and copper-catalyzed addition and substitution reactions of extended multiple bond systems (\u003ci\u003eNorbert Krause and Özge Aksin-Artok\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e18. Copper-mediated cross-coupling reactions (\u003ci\u003eLiza Penn and Dmitri Gelman\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e19. Fluorinated organocopper reagents (\u003ci\u003eCharles R. Davis and Donald J. Burton\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eAuthor index.\u003c\/p\u003e \u003cp\u003eSubject index.\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49525393064279,"sku":"9780470772966","price":1046.85,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9780470772966.jpg?v=1731860343","url":"https:\/\/bookcurl.com\/products\/the-chemistry-of-organocopper-compounds-set-9780470772966","provider":"Book Curl","version":"1.0","type":"link"}