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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 online resource (234 p.) |
| Soggetto topico | Research and information: general |
| Soggetto non controllato |
2,3'-bipyrrole
5-aryl pyrrole-2-carboxylates acylation Al2O3 allosteric modulators arenes borylated aryl alkynes borylation C-C bond forming reactions C-C cross-coupling C-H activation C-H borylation C-H functionalization C-Heteroatom bond forming reactions catalysis in water clinical candidate cross coupling cross-coupling reactions cyclopeptides dearomatization dimerization and trimerization of indoles DNA-encoded libraries DSSC electrophilic haloacetylenes ethynylpyrroles furans Heck reaction heteroarenes heteroaryl substituted pyrroles indigo dyes indolin-3-ones intramolecular cyclization iridium-catalyzed M(CO)3 tripods medium-sized heterocycles methoxycarbonylation molecular brakes and gears n/a NH-Free one-pot reaction palladium profene PROTAC pyrazoles pyrroles restricted rotations Sonogashira cross-coupling spectroscopy styrene sulfonated salan Suzuki coupling Suzuki-Miyaura reaction synthesis thiophenes transition-metal catalysis V-T NMR X-ray |
| 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 online resource (120 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
1-methyl-2-quinolone
1,3-dicarbonyl compound 1,3-Dipole 1,4-dihydropyridines 8-nitro-5-RO-indolizines anchimeric assistance aromaticity C-H functionalization conjugate addition cycloaddition dearomatization Diels-Alder reaction dihydrofuran direct functionalization electron-withdrawing ability electrophilicity enolate epimerization hexapyrrolohexaazacoronene ICT character isoxazoline N-oxide isoxazolo[4,3-b]pyridines nitration nitro nitro group nitroketone nitronate nitropyridines nucleophilic addition nucleophilic substitution nucleophilicity organic materials oxazole-pyrrole ring transformation PDE4 inhibitors perylenediimide Phenacylation of beta-nitropyridin-2-ones pyridone pyrrolidines SNAr substitution total synthesis |
| 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 | ||
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