Investigation of Reactions Involving Pentacoordinate Intermediates

The Mechanism of the Wittig Reaction

  • Peter A. Byrne

Part of the Springer Theses book series (Springer Theses)

Table of contents

About this book

Introduction

In this thesis, the author outlines the discovery of an effect common to representative examples of all Li salt-free Wittig Reactions. The implications of such a universally applicable effect are that all such Wittig reactions occur through the same mechanism. Although the Wittig reaction was first discovered in 1953, its reaction mechanism has never been definitively settled with many different variants proposed and disproved. The work in this thesis shows conclusively that for [2+2] cycloadditions all Wittig reactions occur by the same irreversible mechanism. In addition, the author also describes a new chromatography-free method for the removal of phosphine oxide from the alkene crude product of the Wittig reaction. The work in this thesis has led to several publications in high-profile journals.

Keywords

Alkene Z/E Ratio Kinetic Control in the Wittig Reaction Oxalyl Chloride Oxaphosphetane cis/trans Ration Phosphine Oxide Removal Wittig Reaction Mechanism Ylide Carbonyl [2+2] Cycloaddition

Authors and affiliations

  • Peter A. Byrne
    • 1
  1. 1., School of Chemistry and Chemical BiologyUniversity College DublinDublin 4Ireland

Bibliographic information

  • DOI https://doi.org/10.1007/978-3-642-32045-3
  • Copyright Information Springer-Verlag Berlin Heidelberg 2012
  • Publisher Name Springer, Berlin, Heidelberg
  • eBook Packages Chemistry and Materials Science
  • Print ISBN 978-3-642-32044-6
  • Online ISBN 978-3-642-32045-3
  • Series Print ISSN 2190-5053
  • Series Online ISSN 2190-5061
  • About this book