01000nam0-2200301---450-99001006373040332120160418110908.0001006373FED01001006373(Aleph)001006373FED0100100637320160418d2014----km-y0itay50------baitaIT--------001yyAzioni sperimentali e Sostegno alla famigliaattività svolta a Napoli Norda cura di Angela Palmarelatori: Pietro B. Carrieri, G.Grillo, V.Signoriello, M.T.Gerlini, S.CicalaGiugliano in CampaniaCentro librario Mare Nero201473 p.fot.18 cmFamiglieItaliaPolitiche sociali362.8222itaPalma,Angela748793ITUNINARICAUNIMARCBK990010063730403321362.82 PAL 12662BFSBFSAzioni sperimentali e Sostegno alla famiglia1499100UNINA01121nam a22002891i 450099100375521970753620040607125403.0040802s1959 it a||||||||||||||||ita b13122940-39ule_instARCHE-107555ExLBiblioteca InterfacoltàitaA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l.735Li Rosi, Salvatore490122Li Rosi scultore[S.l.] :Atena,1959[17] c. :ill. ;29 cmPrecedono: L'arte di Salvatore Li Rosi, di A. Neppi; L'uomo, di O. MarcheselliLe interpretazioni liriche delle opere sacre sono di Orazio MarcheselliLi Rosi, SalvatoreOpereCataloghiNeppi, AlbertoMarcheselli, Orazio.b1312294002-04-1405-08-04991003755219707536LE002 Fondo Giudici G 3112002000206138le002C. 1-E0.00-no 00000.i1375863905-08-04Li Rosi scultore308757UNISALENTOle00205-08-04ma -itait 0103496nam 2200817z- 450 991055749400332120210501(CKB)5400000000042891(oapen)https://directory.doabooks.org/handle/20.500.12854/69095(oapen)doab69095(EXLCZ)99540000000004289120202105d2020 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierNitro Compounds and Their Derivatives in Organic SynthesisBasel, SwitzerlandMDPI - Multidisciplinary Digital Publishing Institute20201 online resource (120 p.)3-03943-148-X 3-03943-149-8 Nitro chemistry plays an important role in organic synthesis to construct new frameworks. This is due to the diverse properties of the nitro group. The strong electron-withdrawing ability of the nitro group reduces the electron density of the scaffold, facilitating reactions with nucleophiles or electron transfer. In addition, the -hydrogen of the nitro group is highly acidic, giving a stable anion, which facilitates reactions with both electrophilic and nucleophilic reagents. In addition, the nitro group also serves as a good leaving group, which facilitates transformation to a wide variety of functional groups. Despite the substantial contributions of many researchers, nitro chemistry is still an exciting and challenging research area. This book brings together recent original research and review articles contributed by an international team of leading experts and pioneers in organic synthesis using nitro groups. It is sure to provide useful information and promising insights for researchers.Research & information: generalbicssc1-methyl-2-quinolone1,3-dicarbonyl compound1,3-Dipole1,4-dihydropyridines8-nitro-5-RO-indolizinesanchimeric assistancearomaticityC-H functionalizationconjugate additioncycloadditiondearomatizationDiels-Alder reactiondihydrofurandirect functionalizationelectron-withdrawing abilityelectrophilicityenolateepimerizationhexapyrrolohexaazacoroneneICT characterisoxazoline N-oxideisoxazolo[4,3-b]pyridinesnitrationnitronitro groupnitroketonenitronatenitropyridinesnucleophilic additionnucleophilic substitutionnucleophilicityorganic materialsoxazole-pyrrole ring transformationPDE4 inhibitorsperylenediimidePhenacylation of beta-nitropyridin-2-onespyridonepyrrolidinesSNAr substitutiontotal synthesisResearch & information: generalNishiwaki Nagatoshiedt1294155Nishiwaki NagatoshiothBOOK9910557494003321Nitro Compounds and Their Derivatives in Organic Synthesis3022942UNINA