2019 - Fellow of the American Association for the Advancement of Science (AAAS)
Other disciplines of study, such as Amide and Combinatorial chemistry, are mixed together with her Peptide studies. Helma Wennemers conducts interdisciplinary study in the fields of Combinatorial chemistry and Peptide through her research. Helma Wennemers conducted interdisciplinary study in her works that combined Organic chemistry and Ring (chemistry). She integrates Ring (chemistry) and Organic chemistry in her research. While working in this field, Helma Wennemers studies both Catalysis and Enamine. Her Biochemistry study frequently draws connections between adjacent fields such as Tripeptide. The study of Stereochemistry is intertwined with the study of Collagen helix in a number of ways. She incorporates Collagen helix and Triple helix in her studies. Her research ties Stereochemistry and Triple helix together.
Her Organic chemistry study frequently draws connections between adjacent fields such as Molecule. Her research on Molecule often connects related areas such as Organic chemistry. In her works, she performs multidisciplinary study on Biochemistry and Receptor. She performs multidisciplinary study in Receptor and Biochemistry in her work. Her Stereochemistry study frequently links to other fields, such as Triple helix. Her research is interdisciplinary, bridging the disciplines of Stereochemistry and Triple helix. Her study deals with a combination of Combinatorial chemistry and Peptide. Helma Wennemers merges Peptide with Tripeptide in her study. She performs multidisciplinary study in Catalysis and Stereoselectivity in her work.
Helma Wennemers regularly links together related areas like Amine gas treating in her Organic chemistry studies. In her papers, Helma Wennemers integrates diverse fields, such as Biochemistry and Receptor. Her research on Catalysis frequently connects to adjacent areas such as Addition reaction. Borrowing concepts from Stereoselectivity, Helma Wennemers weaves in ideas under Stereochemistry. In her works, Helma Wennemers conducts interdisciplinary research on Stereoselectivity and Stereochemistry. Helma Wennemers integrates several fields in her works, including Combinatorial chemistry and Organic chemistry. Peptide is closely attributed to Polyproline helix in her study. Her Polyproline helix study frequently draws connections to adjacent fields such as Peptide. She undertakes interdisciplinary study in the fields of Triple helix and Collagen helix through her works.
Helma Wennemers merges many fields, such as Organic chemistry and Combinatorial chemistry, in her writings. Borrowing concepts from Organic chemistry, Helma Wennemers weaves in ideas under Combinatorial chemistry. Catalysis is frequently linked to Addition reaction in her study. Her Biochemistry study frequently draws connections between related disciplines such as Peptide. Her Peptide study frequently draws connections between adjacent fields such as Biochemistry. Helma Wennemers connects Aldol condensation with Aldol reaction in her study. Her multidisciplinary approach integrates Aldol reaction and Aldol condensation in her work. Helma Wennemers undertakes interdisciplinary study in the fields of Solvent and Catalysis through her research. Her research is interdisciplinary, bridging the disciplines of Mathematical analysis and Conjugate.
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Increased structural complexity leads to higher activity: peptides as efficient and versatile catalysts for asymmetric aldol reactions.
Philipp Krattiger;Roman Kovasy;Jefferson D. Revell;Stanislav Ivan.
Organic Letters (2005)
Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins-A Rational Approach
Markus Wiesner;Jefferson D. Revell;Helma Wennemers.
Angewandte Chemie (2008)
Asymmetric catalysis with peptides
Chemical Communications (2011)
Peptide Catalyzed Asymmetric Conjugate Addition Reactions of Aldehydes to Nitroethylene—A Convenient Entry into γ2-Amino Acids
Markus Wiesner;Jefferson D. Revell;Sandro Tonazzi;Helma Wennemers.
Journal of the American Chemical Society (2008)
Enamine Catalysis with Low Catalyst Loadings - High Efficiency via Kinetic Studies
Markus Wiesner;Grégory Upert;Gaetano Angelici;Helma Wennemers.
Journal of the American Chemical Society (2010)
Mimicry of Polyketide Synthases—Enantioselective 1,4‐Addition Reactions of Malonic Acid Half‐Thioesters to Nitroolefins
Jana Lubkoll;Helma Wennemers.
Angewandte Chemie (2007)
Synthetic receptors, libraries and uses thereof
W. Clark Still;Ge Li;Helma Wennemers.
Azidoproline containing helices: stabilization of the polyproline II structure by a functionalizable group.
Michael Kümin;Louis-Sebastian Sonntag;Helma Wennemers.
Journal of the American Chemical Society (2007)
Enantioselective aldol reactions with masked fluoroacetates
Jakub Saadi;Helma Wennemers.
Nature Chemistry (2016)
The “Azido Gauche Effect”Implications for the Conformation of Azidoprolines
Louis-Sebastian Sonntag;Sabine Schweizer;Christian Ochsenfeld;Helma Wennemers.
Journal of the American Chemical Society (2006)
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