Jaap Willem Back, Olivier David, Gertjan Kramer, Géraldine Masson, Piotr T. Kasper, Leo J. de Koning, Luitzen de Jong, Jan H. van Maarseveen, Chris G. de Koster. -quinodimethane formation from benzocyclobutenes triggered by the Staudinger reaction at ambient temperature. It also serves as an alternative way to navigate the website, and as a means of coming up with retrosynthetic ideas. Emandi Ganapathi, Sheri Madhu, Tamal Chatterjee, Rajesh Gonnade, Mangalampalli Ravikanth. The reaction between an azide and triphenylphosphine (or phosphonite) to produce an iminophosphorane (the nucleophilic aza‐ylide) and subsequent hydrolysis to yield a primary amine is generally known as the Staudinger reaction. In contrast to the previous predictions on the relative stability of the unsubstituted cis-configured phosphazide intermediate and the unsubstituted trans-configured phosphazide intermediate, the total energy of the substituted trans-configured phosphazide intermediate is close to that of the substituted cis-configured phosphazide intermediate. Kevin Bläsing, Jonas Bresien, René Labbow, Dirk Michalik, Axel Schulz, Max Thomas, Alexander Villinger. Стеценко. redistribute this material, requesters must process their own requests via the RightsLink permission Polymer-Supported Azidoproazaphosphatrane:  A Recyclable Catalyst for the Room-Temperature Transformation of Triglycerides to Biodiesel. Péter Kele, Xiaohua Li, Martin Link, Krisztina Nagy, András Herner, Krisztián Lőrincz, Szabolcs Béni, Otto S. Wolfbeis. Learn about our remote access options. The reaction between an azide and triphenylphosphine (or phosphonite) to produce an iminophosphorane (the nucleophilic aza‐ylide) and subsequent hydrolysis to yield a primary amine is generally known as the Staudinger reaction.This reaction is a specific, high‐yielding reaction in which the iminophosphorane intermediate hydrolyzes spontaneously in the presence of water. Nicholas M. Hein, Tatsuya Suzuki, Takahiko Ogawa, Michael D. Fryzuk. Adib Charafeddine, Wissam Dayoub, Hubert Chapuis, Peter Strazewski. Please check your email for instructions on resetting your password. Optimized Cartesian coordinates of all the structures at the level of B3LYP/6-31G(d) from Gaussian calculations and relevant molecular orbital diagrams of intermediates, cis and trans, in the Staudinger reactions. Synthesis, structure, spectral, electrochemical and sensing properties of 3-amino boron-dipyrromethene and its derivatives. 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Constantin Mamat, Matthew Gott, Jörg Steinbach. triphenylphosphine phenylimide, is then subjected to hydrolysis to produce a phosphine oxide and an amine: Electronic Supporting Information files are available without a subscription to ACS Web Editions. Citations are the number of other articles citing this article, calculated by Crossref and updated daily. from the ACS website, either in whole or in part, in either machine-readable form or any other form Synthesis of Macrocyclic Lactams from 2-(ω-Aminoalkyl)-2-benzoylamino-3-phenyl-N,N-dimethylpropanamides via Direct Amide Cyclization. Get article recommendations from ACS based on references in your Mendeley library. Filippo Nisic, Gaetano Speciale, Anna Bernardi. Click on the reaction arrow to visit the page. o Tom Desmet, Marc Claeyssens, Kathleen Piens, Wim Nerinckx. Browse other articles of this reference work: The full text of this article hosted at iucr.org is unavailable due to technical difficulties. Bowen Gao, Sigui Chen, Yun Nan Hou, Yong Juan Zhao, Tao Ye, Zhengshuang Xu. Boom, Andrew R. Jupp, Martin Nieger, Andreas W. Ehlers, J. Chris Slootweg. Enantiomeric 2-acetamido-1,4-dideoxy-1,4-iminoribitols as potential pyrrolidine hexosaminidase inhibitors. Aki Kohyama, Eri Koresawa, Kiyoshi Tsuge, Yuji Matsuya. Takahiko Ogawa, Tatsuya Suzuki, Nicholas M. Hein, Fraser S. Pick, Michael D. Fryzuk. An efficient synthesis of phosphoramidates from halides in aqueous ethanol. Stabilization of acyclic phosphazides using the ortho-closo-dicarbadodecaboranyl residue. Alexander Hinz, Axel Schulz, Alexander Villinger, and Jan-Martin Wolter . It also serves as an alternative way to navigate the website, and as a means of coming up with retrosynthetic ideas. Anomalous Staudinger reaction at intramolecular frustrated P–B Lewis pair frameworks. Traceless Staudinger Ligation of Glycosyl Azides with Triaryl Phosphines:  Stereoselective Synthesis of Glycosyl Amides. Sven Fleischmann, Karsten Hinrichs, Ulrich Oertel, Senta Reichelt, Klaus‐Jochen Eichhorn, Brigitte Voit. Balaji V. Rokade, Sanjeev K. Malekar, Kandikere Ramaiah Prabhu. Information about how to use the RightsLink permission system can be found at All systems studied go through a cis-transition state rather than a trans-transition state or a one-step transition state. Marcel Wieland, Jean-Luc Mieusset, Udo H. Brinker. Synthesis, Structure–Activity Relationships, and Preclinical Evaluation of Heteroaromatic Amides and 1,3,4-Oxadiazole Derivatives as 5-HT4 Receptor Partial Agonists.