<div class="csl-bib-body">
<div class="csl-entry">Schnürch, M. (2024, September 24). <i>Solvent free Organic Synthesis - Sustainability through Mechanochemistry</i> [Conference Presentation]. Österreichische Chemietage, Graz, Austria.</div>
</div>
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dc.identifier.uri
http://hdl.handle.net/20.500.12708/208194
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dc.description.abstract
In recent years, mechanochemistry has emerged as a revolutionary tool in modern synthetic chemistry. Especially en route to more sustainable and environmentally benign chemical processes, mechanochemical transformations are privileged, since this approach offers a unique advantage: the ability to conduct conventional synthetic reactions without the need for solvents coupled with rapid reaction kinetics. These unique features make mechanochemistry highly attractive for both industrial applications and fundamental research across diverse fields, including material science, inorganic chemistry, and organic chemistry.
Hence, we started a program to investigate the possibilities for carrying out fundamental organic transformations under solvent free conditions using a mechanochemical setup. Herein we report our results on mechanochemical Tsuji-Trost allylations, Wittig reactions, and Diels-Alder reactions as well as multistep sequences thereof.
en
dc.description.sponsorship
FWF - Österr. Wissenschaftsfonds
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dc.description.sponsorship
European Commission
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dc.language.iso
en
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dc.subject
Mechanochemistry
en
dc.subject
Tsuji Trost Reaction
en
dc.subject
Wittig olefination
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dc.title
Solvent free Organic Synthesis - Sustainability through Mechanochemistry
en
dc.type
Presentation
en
dc.type
Vortrag
de
dc.relation.grantno
P 33064-N
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dc.relation.grantno
860762
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dc.type.category
Conference Presentation
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tuw.project.title
Substitution von gasförmigen Reagenzien durch Feststoffe
