LEADER 01085nam--2200373---450- 001 990003471260203316 005 20101123164531.0 010 $a88-371-0480-4 035 $a000347126 035 $aUSA01000347126 035 $a(ALEPH)000347126USA01 035 $a000347126 100 $a20101123d1990----km-y0itay50------ba 101 $aita 102 $aIT 105 $a||||||||001yy 200 1 $aRetorica della comunicazione nelle letterature classiche$fM.S. Celentano ... [et al.]$g[a cura di Adriano Pennacini] 210 $aBologna$cPitagora Editrice$d1990 215 $aVII,274 p.$d21 cm 410 0$12001 454 1$12001 461 1$1001-------$12001 606 0 $aRetorica classica$xStudi$2BNCF 676 $a803 702 1$aCELENTANO,$bMaria Silvana 702 $aPENNACINI,$bAdriano 801 0$aIT$bsalbc$gISBD 912 $a990003471260203316 951 $aCL 208$b3275 DSA 959 $aBK 969 $aDSA 979 $aDSA$b90$c20101123$lUSA01$h1645 996 $aRetorica della comunicazione nelle letterature classiche$91112157 997 $aUNISA LEADER 03375nam 22006975 450 001 9910917195803321 005 20241209115245.0 010 $a9783031742644 010 $a3031742648 024 7 $a10.1007/978-3-031-74264-4 035 $a(CKB)36959326800041 035 $a(MiAaPQ)EBC31824036 035 $a(Au-PeEL)EBL31824036 035 $a(DE-He213)978-3-031-74264-4 035 $a(OCoLC)1478696361 035 $a(EXLCZ)9936959326800041 100 $a20241209d2024 u| 0 101 0 $aeng 135 $aur||||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aConstruction and Functionalization of Heterocycles by Electrochemistry /$fedited by Eric Nacsa 205 $a1st ed. 2024. 210 1$aCham :$cSpringer Nature Switzerland :$cImprint: Springer,$d2024. 215 $a1 online resource (166 pages) 225 1 $aTopics in Heterocyclic Chemistry,$x1861-9290 ;$v61 311 08$a9783031742637 311 08$a303174263X 327 $aConstruction and derivatization of indole derivatives under electrochemical conditions -- Construction and Functionalization of heterocycles via electrochemical C-H functionalization -- Recent progress in electro-oxidative cross-coupling and annulation -- Electrochemical heterocyclic ring-forming reactions by making C?N and N?N bonds -- Electrochemical (hetero)spirocyclization reactions -- Electrochemical Synthesis and Functionalization of N- and S-heterocycles -- Electrochemical annulation and functionalization of multi-nitrogen-containing heteroaromatics. 330 $aThis book highlights a selection of recent electrochemical approaches to synthesize heterocyclic compounds. Electrochemistry has recently re-emerged as a prevalent technique to promote synthetic organic reactions. This renewed interest arises from its sustainability as well as its ability to engage compounds in unique ways that complement conventional chemical reagents. In the context of heterocyclic synthesis, electrochemistry enables the annulation of simple precursors and the direct functionalization and elaboration of heterocycles, which are the focus of this volume. The primary target audience includes synthetic chemists at all levels of industry and academia. 410 0$aTopics in Heterocyclic Chemistry,$x1861-9290 ;$v61 606 $aOrganic compounds$xSynthesis 606 $aElectrochemistry 606 $aChemical structure 606 $aChemistry, Organic 606 $aGreen chemistry 606 $aSynthetic Chemistry Methodology 606 $aElectrochemistry 606 $aStructure And Bonding 606 $aOrganic Chemistry 606 $aGreen Chemistry 615 0$aOrganic compounds$xSynthesis. 615 0$aElectrochemistry. 615 0$aChemical structure. 615 0$aChemistry, Organic. 615 0$aGreen chemistry. 615 14$aSynthetic Chemistry Methodology. 615 24$aElectrochemistry. 615 24$aStructure And Bonding. 615 24$aOrganic Chemistry. 615 24$aGreen Chemistry. 676 $a547.2 700 $aNacsa$b Eric$01779146 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910917195803321 996 $aConstruction and Functionalization of Heterocycles by Electrochemistry$94302401 997 $aUNINA