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Transition Metal Catalyzed Cross-Coupling Reactions



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Autore: Kostas Ioannis Visualizza persona
Titolo: Transition Metal Catalyzed Cross-Coupling Reactions Visualizza cluster
Pubblicazione: Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica: 1 electronic resource (88 p.)
Soggetto topico: Technology: general issues
Soggetto non controllato: Suzuki-Miyaura cross-couplings
C(sp3) -C(sp2)
alkylboron reagents
metal catalysis
alpha-helix
anode
CH-activation
cross-coupling
electrosynthesis
oligoarene
peptidomimetics
phenol
protein-protein interactions
triflate
thiosemicarbazone
metal complex
transition metal catalysis
cross-coupling reaction
Heck reaction
Suzuki reaction
Sonogashira reaction
Kumada reaction
Buchwald-Hartwig reaction
deposited catalysts
palladium
functional amides
alkynyl ketone synthesis
Persona (resp. second.): KostasIoannis
Sommario/riassunto: Transition metal-catalyzed cross-coupling reactions have proved to be powerful tools for carbon–carbon as well as carbon–heteroatom bond formation in the development of synthetic methodologies for applications ranging from pharmaceuticals to materials. This book, consisting of an editorial, two reviews and two articles, focuses on recent promising research and novel trends in the field of cross-coupling reactions, employing a range of different catalysts. A review by Kostas and Steele provides a survey of the research in the area of cross-coupling catalytic reactions with transition metal complexes based on the thiosemicarbazone unit and a discussion of the prospects for future developments. Another review by Polychronopoulou, Shaya and co-authors describes the progress made over the 21st century concerning the utilization of C(sp3)–organoboranes as partners in metal-catalyzed C(sp3)–C(sp2) cross-couplings, such as B-alkyl Suzuki–Miyaura reactions. The article by Waldvogel, Breinbauer and co-authors demonstrates for the first time the synthetic potential of combining the electro-oxidative dehydrogenative cross coupling of ortho-substituted phenols with Pd-catalyzed cross-coupling reactions. In the second article, Štĕpnička and co-workers describe the preparation of palladium catalysts deposited over silica gel-bearing composite amide-donor functional moieties on the surface, which were evaluated in the Sonogashira-type cross-coupling of acyl chlorides with terminal alkynes.
Titolo autorizzato: Transition Metal Catalyzed Cross-Coupling Reactions  Visualizza cluster
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910557308403321
Lo trovi qui: Univ. Federico II
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