Greenhalgh Iron-Catalysed Hydrofunctionalisation of Alkenes and Alkynes

1. Auflage 2016
ISBN: 978-3-319-33663-3
Verlag: Springer International Publishing
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 306 Seiten, eBook

Reihe: Springer Theses

This thesis gives a thorough account of the development of iron-catalysed hydrosilylation, hydroboration and hydromagnesiation reactions. With extraordinary referencing and scientific argument, Mark Greenhalgh describes the development of methodologies which require only commercially available materials and non-specialised techniques. The intention of this approach is to ensure the science can be adopted widely by the chemical community. In addition to an insight into the processes involved in methodology development, Greenhalgh discusses and determines the relevant reaction mechanisms. This thesis provides not only the most thorough review of the area, but offers a level of insight well beyond that expected from a Ph.D. student. The work in this thesis has been published at the highest level, and the results and ideas have led to 3 industry-funded Ph.D. studentships and grant income in excess of £1 million.

Zielgruppe

Research

Autoren/Hrsg.

Greenhalgh, Mark

Inhaltsverzeichnis

Introduction.- Iron-Catalysed Hydrosilylation of Alkenes and Alkynes.- Iron-Catalysed Hydroboration of Alkenes and Alkynes.- Iron-Catalysed Hydromagnesiation of Styrene Derivatives.- Experimental.- References

Über Autor(innen)

Mark studied Chemistry with a year in Australia at the University of Sheffield, graduating in 2010 after completing his final year project with Dr Simon Jones. He joined the Chemical Synthesis DTC at the University of Bristol in 2010, and began his PhD the following year with Dr Steve Thomas and Prof. Paul Pringle on iron-catalysed hydrofunctionalisation of alkenes and alkynes. He moved with Steve to the University of Edinburgh in 2012 to complete his PhD studies. Mark has recently moved to St. Andrews to work with Prof. Andrew Smith on the development of Lewis base-catalysed asymmetric methodologies.