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 | ||
| Lo trovi qui: Univ. Federico II | ||
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Chiral Auxiliaries and Chirogenesis II
| Chiral Auxiliaries and Chirogenesis II |
| Autore | Borovkov Victor |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (160 p.) |
| Soggetto topico | Research and information: general |
| Soggetto non controllato |
asymmetric synthesis
C-N bond formation chiral ligands chiral resolution chirality circular dichroism circularly polarized luminescence DFT diffusion enantiomeric analysis enantioselective exciton coupling guanidine heterocycles host-guest binding indole induced optical activity magnetochemistry majority-rule mirror symmetry breaking molecular association molecular chirality multinuclear complexes n/a NMR organocatalysis paramagnetic NMR parity violation pillar[5]arene planar chirality polyfluorene polyfluorenevinylene polysilane porphyrin porphyrinoids racemization kinetics self-disproportionation of enantiomers (SDE) self-induced diastereomeric anisochronism (SIDA) sergeants-and-soldiers stereodynamic chirality probe supramolecular chemistry TD-DFT simulation transition-metal catalysis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557757103321 |
Borovkov Victor
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Lo trovi qui: Univ. Federico II | ||
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New Trends in Asymmetric Catalysis
| New Trends in Asymmetric Catalysis |
| Autore | Della Sala Giorgio |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (172 p.) |
| Soggetto topico | Research and information: general |
| Soggetto non controllato |
amines
asymmetric aldol reaction asymmetric catalysis asymmetric synthesis cooperative catalysis electrochemistry enantioselectivity epoxide imines kinetic resolution Lewis acid methanol/water mixtures N-heterocyclic carbenes (NHC) n/a organic electrosynthesis organocatalysis photoredox catalysis proline radical additions radical-radical couplings ring-opening salen complexes stereoselectivity sustainability transition-metal catalysis umpolung umpolung chemistry visible light |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557355803321 |
Della Sala Giorgio
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Lo trovi qui: Univ. Federico II | ||
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