Siegfried R. Waldvogel

Prof. Siegfried R. Waldvogel

Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10−14, 55128 Mainz, Germany
orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
7 March 2018 in Angewandte Chemie International Edition
Verified
Journal Article
Open access
PDF file
AWAnton Wiebe
Anton Wiebe
TGTile Gieshoff
Tile Gieshoff
SMSabine Möhle
Sabine Möhle
EREduardo Rodrigo
Eduardo Rodrigo
MZMichael Zirbes
Michael Zirbes
Siegfried R. WaldvogelSiegfried R. Waldvogel
Siegfried R. Waldvogel
The direct synthetic organic use of electricity is currently experiencing a renaissance. More synthetically oriented laboratories working in this area are exploiting both novel and more traditional concepts, paving the way to broader applications of this niche technology. As only electrons serve as reagents, the generation of reagent waste is efficiently avoided. Moreover, stoichiometric reagents can be regenerated and allow a transformation to be conducted in an electrocatalytic fashion. However, the application of electroorganic transformations is more than minimizing the waste footprint, it rather gives rise to inherently safe processes, reduces the number of steps of many syntheses, allows for milder reaction conditions, provides alternative means to access desired structural entities, and creates intellectual property (IP) space. When the electricity originates from renewable resources, this surplus might be directly employed as a terminal oxidizing or reducing agent, providing an ultra‐sustainable and therefore highly attractive technique. This Review surveys recent developments in electrochemical synthesis that will influence the future of this area.

19 April 2018 in Angewandte Chemie International Edition
Verified
Journal Article
Open access
PDF file
SMSabine Möhle
Sabine Möhle
MZMichael Zirbes
Michael Zirbes
EREduardo Rodrigo
Eduardo Rodrigo
TGTile Gieshoff
Tile Gieshoff
AWAnton Wiebe
Anton Wiebe
Siegfried R. WaldvogelSiegfried R. Waldvogel
Siegfried R. Waldvogel
The use of electricity instead of stoichiometric amounts of oxidizers or reducing agents in synthesis is very appealing for economic and ecological reasons, and represents a major driving force for research efforts in this area. To use electron transfer at the electrode for a successful transformation in organic synthesis, the intermediate radical (cation/anion) has to be stabilized. Its combination with other approaches in organic chemistry or concepts of contemporary synthesis allows the establishment of powerful synthetic methods. The aim in the 21st Century will be to use as little fossil carbon as possible and, for this reason, the use of renewable sources is becoming increasingly important. The direct conversion of renewables, which have previously mainly been incinerated, is of increasing interest. This Review surveys many of the recent seminal important developments which will determine the future of this dynamic emerging field.

2 July 2018 in Chemical Reviews
Verified
Journal Article
Open access
Siegfried R. WaldvogelSiegfried R. Waldvogel
Siegfried R. Waldvogel
SLSebastian Lips
Sebastian Lips
MSMaximilian Selt
Maximilian Selt
BRBarbara Riehl
Barbara Riehl
CKChristopher J. Kampf
Christopher J. Kampf
Arylated products are found in various fields of chemistry and represent essential entities for many applications. Therefore, the formation of this structural feature represents a central issue of contemporary organic synthesis. By the action of electricity the necessity of leaving groups, metal catalysts, stoichiometric oxidizers, or reducing agents can be omitted in part or even completely. The replacement of conventional reagents by sustainable electricity not only will be environmentally benign but also allows significant short cuts in electrochemical synthesis. In addition, this methodology can be considered as inherently safe. The current survey is organized in cathodic and anodic conversions as well as by the number of leaving groups being involved. In some electroconversions the reagents used are regenerated at the electrode, whereas in other electrotransformations free radical sequences are exploited to afford a highly sustainable process. The electrochemical formation of the aryl–substrate bond is discussed for aromatic substrates, heterocycles, other multiple bond systems, and even at saturated carbon substrates. This survey covers most of the seminal work and the advances of the past two decades in this area.

20 May 2020 in Chemical Science
Verified
Journal Article
Open access
PDF file
DPDennis Pollok
Dennis Pollok
Siegfried R. WaldvogelSiegfried R. Waldvogel
Siegfried R. Waldvogel
This perspective provides insight into recent electro-organic methods and general trends in this field, and opens up prospects for future viewpoints.

18 December 2019 in Accounts of Chemical Research
Verified
Journal Article
Closed access
JRJohannes L. Röckl
Johannes L. Röckl
DPDennis Pollok
Dennis Pollok
RFRobert Franke
Robert Franke
Siegfried R. WaldvogelSiegfried R. Waldvogel
Siegfried R. Waldvogel

16 January 2012 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
AKAxel Kirste
Axel Kirste
BEBernd Elsler
Bernd Elsler
GSGregor Schnakenburg
Gregor Schnakenburg
Siegfried R. WaldvogelSiegfried R. Waldvogel
Siegfried R. Waldvogel