LEADER 03616nam 22006735 450 001 9910254023503321 005 20200704014104.0 010 $a3-662-49496-5 024 7 $a10.1007/978-3-662-49496-7 035 $a(CKB)3710000000602244 035 $a(EBL)4428966 035 $a(SSID)ssj0001654193 035 $a(PQKBManifestationID)16433774 035 $a(PQKBTitleCode)TC0001654193 035 $a(PQKBWorkID)14982160 035 $a(PQKB)11405562 035 $a(DE-He213)978-3-662-49496-7 035 $a(MiAaPQ)EBC4428966 035 $a(PPN)192220071 035 $a(EXLCZ)993710000000602244 100 $a20160229d2016 u| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aSustainable C(sp3)-H Bond Functionalization /$fby Jin Xie, Chengjian Zhu 205 $a1st ed. 2016. 210 1$aBerlin, Heidelberg :$cSpringer Berlin Heidelberg :$cImprint: Springer,$d2016. 215 $a1 online resource (91 p.) 225 1 $aSpringerBriefs in Green Chemistry for Sustainability,$x2212-9898 300 $aDescription based upon print version of record. 311 $a3-662-49494-9 320 $aIncludes bibliographical references at the end of each chapters. 327 $aTransition-Metal-Catalyzed, Directing Group Assisted C(sp3)-H Bond Functionalization -- Recent Advances in Non-Directed C(sp3)-H Bond Functionalization -- Functionalization of C(sp3)-H Bond by Visible-Light Photoredox Catalysis. 330 $aThis book highlights major achievements made in the last five years concerning sustainable C(sp3)-H bond functionalization and offers a promising and emerging tool-kit for organic synthesis. The book is divided into three chapters demonstrating key advances in C(sp3)-H bond functionalization. Chapter 1 reviews transition-metal-catalyzed C(sp3)-H bond functionalization using different directing groups, while Chapter 2 addresses the new methods of transition-metal-catalyzed and metal-free C(sp3)-H bond functionalization without directing groups, in addition to briefly highlighting redox-neutral C(sp3)-H bond functionalization. In closing, Chapter 3 examines visible-light photoredox catalysis, an emerging and highly sustainable C(sp3)-H bond functionalization strategy. The book offers an intriguing and useful reference guide for a broad readership working and/or interested in the fields of organic, organometallic, and green chemistry. 410 0$aSpringerBriefs in Green Chemistry for Sustainability,$x2212-9898 606 $aOrganometallic chemistry 606 $aCatalysis 606 $aChemical engineering 606 $aOrganometallic Chemistry$3https://scigraph.springernature.com/ontologies/product-market-codes/C19020 606 $aCatalysis$3https://scigraph.springernature.com/ontologies/product-market-codes/C29000 606 $aIndustrial Chemistry/Chemical Engineering$3https://scigraph.springernature.com/ontologies/product-market-codes/C27000 615 0$aOrganometallic chemistry. 615 0$aCatalysis. 615 0$aChemical engineering. 615 14$aOrganometallic Chemistry. 615 24$aCatalysis. 615 24$aIndustrial Chemistry/Chemical Engineering. 676 $a547.01 700 $aXie$b Jin$4aut$4http://id.loc.gov/vocabulary/relators/aut$01063195 702 $aZhu$b Chengjian$4aut$4http://id.loc.gov/vocabulary/relators/aut 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910254023503321 996 $aSustainable C(sp3)-H Bond Functionalization$92530909 997 $aUNINA