Overview
- Nominated as an outstanding Ph.D. thesis by the University of Toronto, Canada
- Includes extensive background literature on Pd-catalyzed cross-coupling chemistry and catalytic carbon–halogen bond formation
- Presents clear figures and schematics that provide the reader with an intuitive guide
Part of the book series: Springer Theses (Springer Theses)
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Table of contents (4 chapters)
Keywords
About this book
Authors and Affiliations
About the author
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.
Bibliographic Information
Book Title: Stereoselective Heterocycle Synthesis via Alkene Difunctionalization
Book Subtitle: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation
Authors: David A. Petrone
Series Title: Springer Theses
DOI: https://doi.org/10.1007/978-3-319-77507-4
Publisher: Springer Cham
eBook Packages: Chemistry and Materials Science, Chemistry and Material Science (R0)
Copyright Information: Springer International Publishing AG, part of Springer Nature 2018
Hardcover ISBN: 978-3-319-77506-7Published: 10 April 2018
Softcover ISBN: 978-3-030-08472-1Published: 05 January 2019
eBook ISBN: 978-3-319-77507-4Published: 02 April 2018
Series ISSN: 2190-5053
Series E-ISSN: 2190-5061
Edition Number: 1
Number of Pages: XXIX, 365
Number of Illustrations: 155 b/w illustrations, 12 illustrations in colour
Topics: Organometallic Chemistry, Catalysis, Medicinal Chemistry