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Advances in Cross-Coupling Reactions
| Advances in Cross-Coupling Reactions |
| Autore | Pérez Sestelo José |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 electronic resource (234 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
cross coupling
dearomatization C-H functionalization indolin-3-ones dimerization and trimerization of indoles C-H borylation Sonogashira cross-coupling borylated aryl alkynes one-pot reaction restricted rotations M(CO)3 tripods molecular brakes and gears X-ray V-T NMR borylation Suzuki coupling NH-Free 5-aryl pyrrole-2-carboxylates iridium-catalyzed heteroaryl substituted pyrroles 2,3'-bipyrrole electrophilic haloacetylenes pyrroles ethynylpyrroles furans thiophenes pyrazoles Al2O3 transition-metal catalysis intramolecular cyclization medium-sized heterocycles C-H activation acylation palladium arenes heteroarenes indigo dyes DSSC synthesis spectroscopy Heck reaction styrene methoxycarbonylation profene cross-coupling reactions C-C bond forming reactions C-Heteroatom bond forming reactions clinical candidate DNA-encoded libraries cyclopeptides allosteric modulators PROTAC catalysis in water C-C cross-coupling Suzuki-Miyaura reaction sulfonated salan |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557316703321 |
Pérez Sestelo José
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Nitro Compounds and Their Derivatives in Organic Synthesis
| Nitro Compounds and Their Derivatives in Organic Synthesis |
| Autore | Nishiwaki Nagatoshi |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 electronic resource (120 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
nitro
pyridone 1-methyl-2-quinolone cycloaddition direct functionalization perylenediimide nitro group organic materials Phenacylation of beta-nitropyridin-2-ones 8-nitro-5-RO-indolizines oxazole-pyrrole ring transformation conjugate addition dihydrofuran 1,3-dicarbonyl compound enolate isoxazoline N-oxide nitroketone nitronate nucleophilic substitution nitropyridines isoxazolo[4,3-b]pyridines 1,4-dihydropyridines nucleophilic addition Diels-Alder reaction dearomatization hexapyrrolohexaazacoronene nitration SNAr substitution ICT character aromaticity C–H functionalization total synthesis pyrrolidines anchimeric assistance epimerization PDE4 inhibitors 1,3-Dipole electron-withdrawing ability electrophilicity nucleophilicity |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557494003321 |
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Nishiwaki Nagatoshi
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||