2019 - Member of the European Academy of Sciences
Organic chemistry, Combinatorial chemistry, Catalysis, Stereochemistry and Solid-phase synthesis are his primary areas of study. His work in Organic synthesis, Total synthesis, Molecule, Michael reaction and Amination are all subfields of Organic chemistry research. His Molecule study combines topics in areas such as Moiety, Metal-organic framework and Epitaxy.
His Combinatorial chemistry research incorporates elements of Amino acid, Reagent, Vancomycin and Peptide. Stefan Bräse combines subjects such as Crystallography, Biochemistry, Enzyme and Ring with his study of Stereochemistry. Stefan Bräse usually deals with Solid-phase synthesis and limits it to topics linked to Phase and Heck reaction and Linker.
His main research concerns Organic chemistry, Combinatorial chemistry, Stereochemistry, Catalysis and Medicinal chemistry. His Organic chemistry study frequently intersects with other fields, such as Cleavage. His work carried out in the field of Combinatorial chemistry brings together such families of science as Linker, Molecule, Solid-phase synthesis, Triazene and Aryl.
His work on Stereochemistry is being expanded to include thematically relevant topics such as Ligand. Stefan Bräse is involved in the study of Catalysis that focuses on Palladium in particular.
Stefan Bräse mostly deals with Combinatorial chemistry, Medicinal chemistry, Catalysis, Stereochemistry and Polymer. His Combinatorial chemistry study incorporates themes from Peptoid, Enantioselective synthesis, Alkyne, Azide and Aryl. He interconnects Mass spectrum, Mass spectrometry, Quinoline, Regioselectivity and Triethylamine in the investigation of issues within Medicinal chemistry.
Stefan Bräse has included themes like Cobalt, Reagent and Metal in his Catalysis study. Stefan Bräse mostly deals with Chirality in his studies of Stereochemistry. His research integrates issues of Linker, Nanotechnology and Chemical engineering in his study of Polymer.
His primary scientific interests are in Combinatorial chemistry, Nanotechnology, OLED, Photochemistry and Polymer. The concepts of his Combinatorial chemistry study are interwoven with issues in Green chemistry, Catalysis, Enantioselective synthesis, Stokes shift and Alkyl. His Nanotechnology research includes themes of Surface modification and Metal-organic framework.
His OLED research is multidisciplinary, relying on both Luminescence, Triplet state, Molecule and Electroluminescence. The study incorporates disciplines such as Azide, Curtius rearrangement, Chemical engineering and Cycloaddition in addition to Polymer. His study with Aryl involves better knowledge in Organic chemistry.
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Organic Azides: An Exploding Diversity of a Unique Class of Compounds
Stefan Bräse;Carmen Gil;Kerstin Knepper;Viktor Zimmermann.
Angewandte Chemie (2005)
Chemistry, Biology, and Medicine of the Glycopeptide Antibiotics.
K. C. Nicolaou;Christopher N. C. Boddy;Stefan Bräse;Nicolas Charles Winssinger.
Angewandte Chemie (1999)
Porous Polymer Networks: Synthesis, Porosity, and Applications in Gas Storage/Separation
Weigang Lu;Daqiang Yuan;Dan Zhao;Christine Inge Schilling.
Chemistry of Materials (2010)
Chemistry and Biology of Mycotoxins and Related Fungal Metabolites
Stefan Bräse;Arantxa Encinas;Julia Keck;Carl F. Nising.
Chemical Reviews (2009)
Organic azides : syntheses and applications
Stefan Bräse;Klaus Banert.
The oxa-Michael reaction: from recent developments to applications in natural product synthesis
Carl F. Nising;Stefan Bräse.
Chemical Society Reviews (2008)
Metal-Catalyzed Cross-Coupling Reactions and More: DeMeijere/Metal-Catalyzed Cross-Coupling Reactions and More
Armin de Meijere;Stefan Bräse;Martin Oestreich.
Recent developments in the field of oxa-Michael reactions
Carl F. Nising;Stefan Bräse.
Chemical Society Reviews (2012)
Recent approaches towards the asymmetric synthesis of α,α-disubstituted α-amino acids
Henning Vogt;Stefan Bräse.
Organic and Biomolecular Chemistry (2007)
Metal-catalyzed cross-coupling reactions and more
A. de Meijere;Stefan Bräse;Martin Oestreich.
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