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| Autore: |
D'Errico Stefano
|
| Titolo: |
Molecules from Side Reactions
|
| Pubblicazione: | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica: | 1 online resource (100 p.) |
| Soggetto topico: | History of engineering and technology |
| Soggetto non controllato: | (E,Z)-isomerization |
| 19F NMR spectroscopy | |
| 1H-pyrazolo[3,4-b]pyridine | |
| 3-acetyl-2,3-dihydro-1,3,4-oxadiazole | |
| 8-Fluoro-2'-deoxyguanosine | |
| acadesine | |
| AICAR | |
| allenic compounds | |
| AMPK | |
| azaheterocycles | |
| benzamides | |
| bidentate directing groups | |
| bis-chelates | |
| C-glycosylation | |
| C-H bond functionalization | |
| caprazamycins | |
| carbohydrate | |
| chelation assistance | |
| chlorinated nucleosides | |
| conjugated diyne | |
| copper | |
| cyanide | |
| cyclization | |
| diacetal | |
| epoxide | |
| ester group migration | |
| fluorinated nucleosides | |
| fluorination | |
| furan | |
| glycosyl sulfoxide | |
| guanidinium | |
| heterocycle | |
| hydroxy methylation | |
| ketose | |
| LAH reduction | |
| ligand | |
| mannose | |
| modified nucleosides | |
| muraymycins | |
| N-alkylation | |
| N-C bond cleavage | |
| N'-acetylhydrazide | |
| n/a | |
| network | |
| nitration | |
| nucleoside analogues | |
| nucleosides | |
| organic synthesis | |
| oxazole | |
| oxetane | |
| pent-1,2,3,4-tetraene intermediate | |
| phosphoramidite | |
| phosphorylation | |
| psicose | |
| pyridine derivatives | |
| pyridine-imidazolium | |
| rare sugar | |
| rearrangement | |
| ribose | |
| RORC reaction | |
| seven-membered rings | |
| solid phase synthesis | |
| spiro-oxetane | |
| thioglycoside oxidation | |
| unexpected iminium cation | |
| uridine | |
| uronate | |
| X-ray structure determination | |
| Persona (resp. second.): | D'ErricoStefano |
| Sommario/riassunto: | The Special Issue "Molecules from Side Reactions" is a collection of papers reporting on the synthesis and characterization of the molecules that come from unexpected synthetic routes. This is the first example of a Special Issue based on such a topic, notwithstanding that all synthetic chemists have isolated a side product during a chemical reaction. Instead of continuing to store the side products in the freezer, I have thought to give them the dignity of publication, making them available to the scientific community. The short manuscripts collected here respect the principle of "one compound per paper" and have the purpose of preserving the molecular diversity deriving from a chemical reaction. The molecular scaffolds are unexpected and intriguing, and could be useful starting points or intermediates for exploring novel reactions. |
| Titolo autorizzato: | Molecules from Side Reactions ![]() |
| Formato: | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione: | Inglese |
| Record Nr.: | 9910674046603321 |
| Lo trovi qui: | Univ. Federico II |
| Opac: | Controlla la disponibilità qui |