Search Results - "Revell, Jefferson D"

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  1. 1

    Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins-A Rational Approach by Wiesner, Markus, Revell, Jefferson D, Wennemers, Helma

    Published in Angewandte Chemie (International ed.) (22-02-2008)
    “…Bridging the gap: Conformational analysis of a peptidic catalyst for aldol reactions led to the development of H‐D‐Pro‐Pro‐Asp‐NH2 as a highly efficient…”
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    Journal Article
  2. 2

    Increased Structural Complexity Leads to Higher Activity:  Peptides as Efficient and Versatile Catalysts for Asymmetric Aldol Reactions by Krattiger, Philipp, Kovasy, Roman, Revell, Jefferson D, Ivan, Stanislav, Wennemers, Helma

    Published in Organic letters (17-03-2005)
    “…Peptides containing a secondary amine and a carboxylic acid in a specific orientation to each other are presented as highly efficient catalysts for asymmetric…”
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  3. 3

    Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H-Pro-Pro-Asp-NH2? by Revell, JeffersonD., Wennemers, Helma

    Published in Advanced synthesis & catalysis (05-05-2008)
    “…H‐Pro‐Pro‐Asp‐NH2 1 is a versatile catalyst for asymmetric aldol reactions. Within the catalyst structure, both the N‐terminal secondary amine and the…”
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  4. 4

    Peptidic catalysts developed by combinatorial screening methods by Revell, Jefferson D, Wennemers, Helma

    Published in Current opinion in chemical biology (01-06-2007)
    “…In recent years, oligopeptides have been developed as efficient catalysts for a range of important organic reactions, including acylation, silylation,…”
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  5. 5

    Is more better? A comparison of tri- and tetrapeptidic catalysts by Schnitzer, Tobias, Wiesner, Markus, Krattiger, Philipp, Revell, Jefferson D, Wennemers, Helma

    Published in Organic & biomolecular chemistry (19-07-2017)
    “…From an enzymatic perspective, there is a general notion that the bigger and more complex a catalytically active peptide is the more enzyme-like and the better…”
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  6. 6

    Stapled Vasoactive Intestinal Peptide (VIP) Derivatives Improve VPAC2 Agonism and Glucose-Dependent Insulin Secretion by Giordanetto, Fabrizio, Revell, Jefferson D, Knerr, Laurent, Hostettler, Marie, Paunovic, Amalia, Priest, Claire, Janefeldt, Annika, Gill, Adrian

    Published in ACS medicinal chemistry letters (12-12-2013)
    “…Agonists of vasoactive intestinal peptide receptor 2 (VPAC2) stimulate glucose-dependent insulin secretion, making them attractive candidates for the treatment…”
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    Ionic Liquid Acceleration of Solid-Phase Suzuki−Miyaura Cross-Coupling Reactions by Revell, Jefferson D, Ganesan, A

    Published in Organic letters (05-09-2002)
    “…Room-temperature ionic liquids promote various transition metal-catalyzed reactions in the solution phase. Here, for the first time, we show that these effects…”
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  9. 9

    Solid-supported and pegylated H-Pro-Pro-Asp-NHR as catalysts for asymmetric aldol reactions by Revell, Jefferson D., Gantenbein, Daniel, Krattiger, Philipp, Wennemers, Helma

    Published in Biopolymers (2006)
    “…H–Pro–Pro–Asp–NH2 is a highly active and selective catalyst for asymmetric aldol reactions. Here, the versatility of H–Pro–Pro–Asp–NH2 has been further…”
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  10. 10

    Separating stereoisomers of di-, tri-, and tetrapeptides using capillary electrophoresis with contactless conductivity detection by Gong, Xiao Yang, Dobrunz, Dominik, Kümin, Michael, Wiesner, Markus, Revell, Jefferson D, Wennemers, Helma, Hauser, Peter C

    Published in Journal of separation science (01-02-2008)
    “…The separation and detection of small oligopeptides in CE with contactless conductivity detection were demonstrated. A strongly acidic separation buffer (0.5 M…”
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  11. 11

    Peptide–polyethylene glycol conjugates: Synthesis and properties of peptides bearing a C-terminal polyethylene glycol chain by Grun, Jessica, Revell, Jefferson D., Conza, Matteo, Wennemers, Helma

    Published in Bioorganic & medicinal chemistry (15-09-2006)
    “…The introduction of a polyethylene glycol chain has become a popular tool for increasing water solubility and bioavailability. Our interest in the development…”
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  12. 12

    Peptide Catalyzed Asymmetric Conjugate Addition Reactions of Aldehydes to Nitroethylene—A Convenient Entry into γ2-Amino Acids by Wiesner, Markus, Revell, Jefferson D, Tonazzi, Sandro, Wennemers, Helma

    Published in Journal of the American Chemical Society (30-04-2008)
    “…The peptide H-d-Pro-Pro-Glu-NH2 is a highly effective catalyst for conjugate addition reactions between aldehydes and nitroethylene. Only 1 mol % of…”
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  13. 13

    PS-COD and PS-9-BBN:  Polymer-Supported Reagents for Solution-Phase Parallel Synthesis by Revell, Jefferson D, Dörner, Barbara, White, Peter D, Ganesan, A

    Published in Organic letters (03-03-2005)
    “…1,5-Cyclooctadiene was deprotonated under LICKOR conditions and reacted with Merrifield resin to afford an immobilized cyclooctadiene in high yield. This…”
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  14. 14

    Synthesis of Functionalized 1,5-Cyclooctadienes by LICKOR Metalation by Revell, Jefferson D, Ganesan, A

    Published in Journal of organic chemistry (23-08-2002)
    “…1,5-Cyclooctadiene was lithiated under LICKOR superbase conditions followed by reaction with alkyl halides or ethylene oxide to yield 3-substituted…”
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  15. 15

    Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins-A Rational Approach by Wiesner, Markus, Revell, JeffersonD., Wennemers, Helma

    Published in Angewandte Chemie (22-02-2008)
    “…Geplante Abstände: Basierend auf der Konformationsanalyse eines peptidischen Katalysators für Aldolreaktionen wurde das Peptid H‐D‐Pro‐Pro‐Asp‐NH2 als ein hoch…”
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    Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H‐Pro‐Pro‐Asp‐NH 2 ? by Revell, JeffersonD., Wennemers, Helma

    Published in Advanced synthesis & catalysis (05-05-2008)
    “…Abstract H‐Pro‐Pro‐Asp‐NH 2 1 is a versatile catalyst for asymmetric aldol reactions. Within the catalyst structure, both the N‐terminal secondary amine and…”
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  19. 19

    Functional group requirements within the peptide H-Pro-Pro-Asp-NH 2 as a catalyst for aldol reactions by Revell, Jefferson D., Wennemers, Helma

    Published in Tetrahedron (2007)
    “…H-Pro-Pro-Asp-NH 2 1 is a versatile catalyst for asymmetric aldol reactions. In this work, the functional group tolerance within the catalyst structure has…”
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  20. 20

    Using Catalyst-Substrate Coimmobilization for the Discovery of Catalysts for Asymmetric Aldol Reactions in Split-and-Mix Libraries by Krattiger, Philipp, Kovàsy, Roman, Revell, JeffersonD., Wennemers, Helma

    Published in QSAR & combinatorial science (01-12-2005)
    “…“Catalyst–substrate coimmobilization” has been used for the discovery of highly active and selective peptidic catalysts for asymmetric aldol reactions within…”
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