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Iron-Catalyzed Synthesis of Fused Aromatic Compounds via C¿H Bond Activation
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Artikel-Nr:
9784431549277
Veröffentl:
2014
Einband:
HC runder Rücken kaschiert
Erscheinungsdatum:
25.07.2014
Seiten:
88
Autor:
Arimasa Matsumoto
Gewicht:
307 g
Format:
241x160x11 mm
Serie:
Springer Theses
Sprache:
Englisch
Beschreibung:
Iron catalysts in organic synthesis are strongly in demand because iron is non-toxic, inexpensive and the most abundant transition metal in the earth, although their use is still limited compared with that of rare, precious metals such as palladium, ruthenium and rhodium. This thesis describes the first practical example of iron catalysis in the carbon hydrogen bond activation reaction to synthesized fused aromatic ring compounds. By using a unique combination of iron catalyst and dichloride oxidant, various kind of naphthalene and phenanthrene derivatives were synthesized via annulation reaction with alkynes including direct C H bond activation process. This achievement opens the new possibility of low-valent iron catalysis and expands synthetic methods for a sustainable society.
Nominated by The University of Tokyo as an outstanding Ph.D. thesis
General Introduction.- Iron-Catalyzed Naphthalene Synthesis from Alkyne and Grignard Reagent.- Iron-Catalyzed Phenanthrene Synthesis from Alkyne and Grignard Reagent.- Iron-Catalyzed Phenanthrene Synthesis from Alkyne and Aryl Bromide Mediated by Metallic Magnesium.- Summary and Perspectives.