C-P and C-C Bond Forming Reactions Based on Carbostyrils and Thioamide

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This guide is based on the synthesis of bisquinlone based phosphine ligands and desulfitative carbon-carbon bond forming reactions. It is divided into 3 chapters which include first an overview about heterocyclic BINAP analogues. In this chapter, survey of developing atropisomeric biheteroaryl backbone-containing bisphosphines, their designing concept, synthetic approaches and some of their important applications are discussed. Second, efficient synthesis of functionalized novel bisquinolone based mono- and diphosphine ligands of the aza-BINAP type. Preliminary studies confirm that these novel types of aza-BINAP phosphines containing an enamide moiety incorporated into the heteroaryl ring are indeed useful ligands in transition metal-catalyzed transformations. Third, palladium(0)- catalyzed, copper(I)-mediated desulfitative C C cross-coupling protocol (Liebeskind Srogl type) of cyclic thioamides and thioureas with alkenylboronic acids, vinyl- and (het)arylstannanes, and arylsiloxanes is performed. These C C cross-couplings are a valuable extension of the traditional Liebeskind Srogl reactions utilizing thioethers as electrophilic reagents.

Autorentext

Dr.Nuzhat Arshad conducted her doctoral studies (2006-2009) on the synthesis of microwave assisted homogenous/heterogenous catalysis/combinatorial chemistry/bio-active compounds synthesis at University of Graz, Austria under the supervision of Prof. C. Oliver Kappe. She has also expertise in isolation of natural products & microbial transformations

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Weitere Informationen

  • Allgemeine Informationen
    • GTIN 09783639256604
    • Sprache Englisch
    • Genre Chemie
    • Größe H220mm x B220mm
    • Jahr 2010
    • EAN 9783639256604
    • Format Kartonierter Einband (Kt)
    • ISBN 978-3-639-25660-4
    • Titel C-P and C-C Bond Forming Reactions Based on Carbostyrils and Thioamide
    • Autor Nuzhat Arshad
    • Untertitel Phosphine Ligands and Thioamide Derivatives
    • Herausgeber VDM Verlag Dr. Müller e.K.
    • Anzahl Seiten 92

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