Stereoselective Heterocycle Synthesis via Alkene Difunctionalization

Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation

David A. Petrone (Autor)

Buch | Hardcover

XXIX, 365 Seiten

2018 | 1st ed. 2018
Springer International Publishing (Verlag)
978-3-319-77506-7 (ISBN)

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This book investigates the use of palladium modified by bulky ligands as catalysts for new chemical transformations that rapidly assemble several classes of complex heterocyles. It documents the development of new chemical reactions involving carbon-carbon (C-C) and carbon-halogen (C-X) bond formation in the context of alkene difunctionalization and dearomatization reactions. Due to the ubiquity of heterocycles in bioactive natural products and life-improving pharmaceutical treatments, a long-term goal for synthetic organic chemists has been to develop novel and creative heterocycle syntheses that illicit a high degree of product diversity and are characterized by mild reaction conditions and limited waste production. A considerable fraction of leading pharmaceutical drugs contain at least one heterocycle within their chemical structure, and their prevalence in these technologies is strong evidence that the fundamental curiosities of organic chemistry lead to real-world solutions for the health and wellness of the global population.

David A. Petrone was born in Scarborough, Canada in 1989. He obtained his B.Sc. in Chemistry with Honors from the University of Guelph in 2011 and his Ph.D. in 2016 from the University of Toronto under the supervision of Prof. Mark Lautens. He was awarded both the Boehringer Ingelheim Award of Excellence in Organic Chemistry and the Chair's Doctoral Medal for the work contained in this thesis. He is currently an NSERC postdoctoral fellow in Prof. Erick M. Carreira's group at the Laboratory of Organic Chemistry at the ETH Zürich.

Diastereoselective Synthesis of Heterocycles via Intramolecular Pd-Catalyzed Alkene Aryliodination.- Pd-Catalyzed Diastereoselective Carbocyanation Reactions of Chiral N -Allyl Carboxamides and Indoles.- Development of a Pd-Catalyzed Dearomative 1,2-Diarylation of Indoles using Aryl Boron Reagents.- Harnessing Reversible Oxidative Addition: Application of Diiodinated Aromatic Compounds in Aryliodination.

Erscheinungsdatum	21.04.2018
Reihe/Serie	Springer Theses
Zusatzinfo	XXIX, 365 p. 167 illus., 12 illus. in color.
Verlagsort	Cham
Sprache	englisch
Maße	155 x 235 mm
Gewicht	754 g
Themenwelt	Medizin / Pharmazie ► Pharmazie
	Naturwissenschaften ► Biologie ► Biochemie
	Naturwissenschaften ► Chemie ► Organische Chemie
	Naturwissenschaften ► Chemie ► Physikalische Chemie
Schlagworte	Catalyst Development • Cyanation Reactions • Halogenation Reactions • Heck Reaction • Natural Product Synthesis • Palladium Catalysis • Phosphine Ligands • Reaction Progress • Stereoselective Synthesis • Suzuki Coupling
ISBN-10	3-319-77506-5 / 3319775065
ISBN-13	978-3-319-77506-7 / 9783319775067
Zustand	Neuware