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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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Feature Papers in Compounds
| Feature Papers in Compounds |
| Autore | Mejuto Juan C |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (234 p.) |
| Soggetto topico |
Technology: general issues
Chemical engineering |
| Soggetto non controllato |
atropisomerism
4,4'-bipyridine pyridine N-oxidation halogenation halogen bond cyanation Finkelstein reaction Suzuki coupling Orchis scent gas chromatography mass spectrometry solid-phase microextraction quantum chemistry computational chemistry molecular dynamics modeling open-source software proprietary software Himantoglossum solid phase microextraction iodination alkanes alkenes alkynes alkyl carbonyls elemental iodine iodides Zutano variety avocado oil Soxhlet extraction ultrasound-assisted extraction volatiles ripening over-ripe HS-SPME-GC-MS Basilicata Barlia robertiana Himantoglossum robertianum mantel test Orchidaceae pollination syndrome Italy volatile compounds solvolysis aryldiazonium ions perchlorate anions silicon carbide (SiC) 3C-SiC powder 4H-SiC crystal impurities photoluminescence pnictogen bonding nitrogen as pnictogen bond donor geometries crystal structure analysis ICSD and CSD database analyses MESP characterizations sum of the van der Waals radii concept Dactylorhiza volatile organic compounds thiosemicarbazone metal complexes DNA interactions biological activity thiazolidinedione microwave synthesis compound library rosiglitazone Knoevangel condensation biodiesel production crude glycerin carbon materials |
| ISBN | 3-0365-5988-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910639987403321 |
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Mejuto Juan C
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| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Modern Strategies for Heterocycle Synthesis
| Modern Strategies for Heterocycle Synthesis |
| Autore | Favi Gianfranco |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 electronic resource (372 p.) |
| Soggetto topico | Medicine |
| Soggetto non controllato |
amine nucleophiles
alkynoic acids cascade reaction gold catalysis fused N-heterocycles solid-phase synthesis ketone traceless synthesis natural products enol ethers photocatalysis photoredox visible-light-induced catalysis photoredox cyclization organic dyes heterocycles dihydrocoumarins synthesis 3-trifluoroacetyl coumarins phenols antifungal activities terpyridines 3,2':6',3"-terpyridine cyclohexanol derivative condensation heterocyclic 1,2,3-triazol triazolylmethyl phosphinate triazolylmethyl phosphate copper-catalyzed azide-alkyne cycloaddition click reaction azides cinnolines triazoles CuAAC alkynes cycloalkynes Richter cyclization Suzuki coupling fluorescence cytotoxicity coumarin pyrazolo[3,4-b]pyridine silica sulfuric acid 2H-pyran valence isomerism 1-oxa-triene dienone oxa-electrocyclization Knoevenagel propargyl Claisen cycloisomerization asymmetric dimeric β-carboline acylhydrazone group cytotoxic antitumor structure-activity relationship γ-lactam pyrrolidones multicomponent reactions organocatalysis pyridine CF3CO-acetylenes 1,3-oxazines fluorinated heterocycles saturated oxygen heterocycles cyclic ethers total synthesis multicomponent reaction α-halohydrazones Staudinger reaction aza-Wittig 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine purine nucleobase aromatic substitution arylation fluoroalcohol α-chloroglycinates 5-acylamino-1,3-thiazoles Hantzsch reaction TMSBr propargylic alcohols cascade cyclization 4-bromo quinolines synthesis of benzofurans intra-molecular approach inter-molecular approach |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557409903321 |
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Favi Gianfranco
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Supramolecular Gold Chemistry : From Atomically Precise Thiolate-Protected Gold Nanoclusters to Gold-Thiolate Nanostructures
| Supramolecular Gold Chemistry : From Atomically Precise Thiolate-Protected Gold Nanoclusters to Gold-Thiolate Nanostructures |
| Autore | Antoine Rodolphe |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 electronic resource (182 p.) |
| Soggetto topico | Technology: general issues |
| Soggetto non controllato |
alloy
metal exchange atomically precise gold nanoclusters thiolate catenane ion mobility DFT calculations gold nanocluster cross-coupling Ullmann hetero-coupling Sonogashira coupling Suzuki coupling A3−coupling catalytic mechanism ligand removal gold nanomaterials electron dynamics phonon dynamics optical properties Au70S20(PPh3)12 cluster superatom network model electronic structure geometric structure gold nanoparticles graphene oxide laser ablation Au-GO nano-hybrid coordination polymer structure amino acids template-assisted synthesis fluorescence Au(I)-thiolate gold nanohybrid materials 3-MBA/Au MPCs TEA-HFIP ESI-MS HPLC-MS bidentate binding gold thiolate coordination polymer lamellar structure luminescence polymer composite gold cluster catalyst hydrogen evolution reaction oxygen evolution reaction oxygen reduction reaction water splitting fuel cells ligand-protected photoluminescence mechanism metal nanoclusters quantum confinement effect ligand effect p band intermediate state (PBIS) interface state nanocatalysis 6-aza-2-thio-thymine protein |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Supramolecular Gold Chemistry |
| Record Nr. | UNINA-9910557146903321 |
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Antoine Rodolphe
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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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