Single Electron Transfer‐Induced Selective α˗Oxygenation of Glycine Derivatives
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U. Jahn | I. Císařová | Navyasree Venugopal | Burkhard Koenig | Margaréta Vojtičková | Johannnes Moser
[1] Stephen J. Walsh,et al. Photocatalytic methods for amino acid modification. , 2020, Chemical Society reviews.
[2] C. Vila,et al. Asymmetric Oxidative Mannich Reactions , 2020 .
[3] Adrián Gómez‐Suárez,et al. Radikal‐basierte Synthese und Modifikation von Aminosäuren , 2020 .
[4] Rongli Zhang,et al. Site-selective and diastereoselective functionalization of α-amino acid and peptide derivatives via palladium-catalyzed sp3 C–H activation , 2020 .
[5] V. I. Maleev,et al. Advances in Asymmetric Amino Acid Synthesis Enabled by Radical Chemistry , 2020 .
[6] Adrián Gómez‐Suárez,et al. Radical‐Based Synthesis and Modification of Amino Acids , 2020, Angewandte Chemie.
[7] jin-quan yu,et al. From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C-H Functionalization Reactions. , 2020, Accounts of chemical research.
[8] Ge Qu,et al. Die zentrale Rolle der Methodenentwicklung in der gerichteten Evolution selektiver Enzyme , 2020 .
[9] Ge Qu,et al. The Crucial Role of Methodology Development in Directed Evolution of Selective Enzymes. , 2020, Angewandte Chemie.
[10] A. Studer,et al. Der “Persistent Radical Effect” in der organischen Chemie , 2020, Angewandte Chemie.
[11] A. Studer,et al. The Persistent Radical Effect in Organic Synthesis. , 2019, Angewandte Chemie.
[12] M. Kanai,et al. Synthetic Methodology-driven Chemical Protein Modifications , 2019, Chemistry Letters.
[13] U. Kazmaier,et al. Peptide Modifications: Versatile Tools in Peptide and Natural Product Syntheses , 2019, Synlett.
[14] B. G. Davis,et al. Concepts of Catalysis in Site-Selective Protein Modifications , 2019, Journal of the American Chemical Society.
[15] M. Reetz. Directed Evolution of Artificial Metalloenzymes: A Universal Means to Tune the Selectivity of Transition Metal Catalysts? , 2019, Accounts of chemical research.
[16] Peter G. Jones,et al. Diastereoselective Radical Couplings Enable the Asymmetric Synthesis of anti -β-Amino-α-hydroxy Carboxylic Acid Derivatives , 2018, European Journal of Organic Chemistry.
[17] R. Pohl,et al. Unique Stereoselective Homolytic C-O Bond Activation in Diketopiperazine-Derived Alkoxyamines by Adjacent Amide Pyramidalization. , 2018, Chemistry.
[18] Sushobhan Chowdhury,et al. Recent Advances on Amino Acid Modifications via C–H Functionalization and Decarboxylative Functionalization Strategies , 2018 .
[19] Frances H. Arnold. Gerichtete Evolution: Wie man neue Chemie zum Leben erweckt , 2018 .
[20] Frances H Arnold,et al. Directed Evolution: Bringing New Chemistry to Life , 2017, Angewandte Chemie.
[21] Łukasz Berlicki,et al. Sequence Engineering to Control the Helix Handedness of Peptide Foldamers. , 2017, Chemistry.
[22] A. Madder,et al. Chemical Protein Modification through Cysteine , 2016, Chembiochem : a European journal of chemical biology.
[23] Tynchtyk Amatov,et al. Synthese überbrückter Diketopiperazine mit Hilfe des persistenten Radikaleffekts und eine formale Synthese von Bicyclomycin , 2015 .
[24] R. Pohl,et al. Synthesis of bridged diketopiperazines by using the persistent radical effect and a formal synthesis of bicyclomycin. , 2015, Angewandte Chemie.
[25] Jonas S. Laursen,et al. β-Peptoid Foldamers at Last. , 2015, Accounts of chemical research.
[26] Hans Renata,et al. Ausdehnung des Enzym‐Universums: Zugang zu nicht‐natürlichen Reaktionen durch mechanismusgeleitete, gerichtete Evolution , 2015 .
[27] Frances H Arnold,et al. Expanding the enzyme universe: accessing non-natural reactions by mechanism-guided directed evolution. , 2015, Angewandte Chemie.
[28] Gonçalo J L Bernardes,et al. Advances in chemical protein modification. , 2015, Chemical reviews.
[29] B. König,et al. Photocatalytic α‐Oxyamination of Stable Enolates, Silyl Enol Ethers, and 2‐Oxoalkane Phosphonic Esters , 2015 .
[30] U. Jahn,et al. General and Efficient α‐Oxygenation of Carbonyl Compounds by TEMPO Induced by Single‐Electron‐Transfer Oxidation of Their Enolates , 2012 .
[31] F. Fülöp,et al. Peptidic foldamers: ramping up diversity. , 2012, Chemical Society reviews.
[32] A. F. Zahoor,et al. A straightforward approach towards combined α-amino and α-hydroxy acids based on Passerini reactions , 2011, Beilstein journal of organic chemistry.
[33] A. Kristensen,et al. Cell-permeable and plasma-stable peptidomimetic inhibitors of the postsynaptic density-95/N-methyl-D-aspartate receptor interaction. , 2011, Journal of medicinal chemistry.
[34] B. G. Davis,et al. Olefin Metathesis for Site‐Selective Protein Modification , 2009, Chembiochem : a European journal of chemical biology.
[35] U. Kazmaier,et al. Peptide Backbone Modifications , 2008 .
[36] H. Sajiki,et al. Solvent-modulated Pd/C-catalyzed deprotection of silyl ethers and chemoselective hydrogenation , 2004 .
[37] J. Rokach,et al. Silyl group deprotection by Pd/C/H2. A facile and selective method , 2004 .
[38] Peter Blakskjaer,et al. Studies on the C-alkylation and C-allylation of small peptides employing glycyl radical intermediates , 2001 .
[39] T. Skrydstrup,et al. Selective Side Chain Introduction onto Small Peptides Mediated by Samarium Diiodide: A Potential Route to Peptide Libraries , 2000 .
[40] Samuel H. Gellman,et al. Foldamers: A Manifesto , 1998 .
[41] C. Easton. Free-Radical Reactions in the Synthesis of alpha-Amino Acids and Derivatives. , 1997, Chemical reviews.
[42] H. Hiemstra,et al. Xanthate transfer addition of a glycine radical equivalent to alkenes; a novel route to a-amino acid derivates. , 1994 .
[43] D. Seebach,et al. Peptide Enolates. C-Alkylation of Glycine Residues in linear tri-, tetra-, and pentapeptides via dilithium azadienediolates , 1994 .
[44] D. Seebach,et al. Modification of Cyclosporin A (CS): Generation of an enolate at the sarcosine residue and reactions with electrophiles , 1993 .
[45] D. Seebach,et al. C-alkylation of peptides through polylithiated and LiCl-solvated derivatives containing sarcosine Li-enolate units , 1991 .
[46] C. Easton,et al. Selective reaction of glycine residues in hydrogen atom transfer from amino acid derivatives , 1989 .
[47] C. Easton,et al. Preferential reactivity of glycine residues in free radical reactions of amino acid derivatives , 1986 .
[48] J. Sperling,et al. Photochemical modification of glycine-containing polypeptides , 1971 .
[49] D. Elad,et al. Photoalkylation of glycine derivatives , 1965 .