Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Contact Nasser Iranpoor, Habib Firouzabadi, Dariush Khalili. Customer Service, © 2020 Merck KGaA, Darmstadt, Germany and/or its affiliates. Users are Enantioselective Total Syntheses of (−)-Palau’amine, (−)-Axinellamines, and (−)-Massadines. Paola Agrigento, Fernando Albericio, Sylvie Chamoin, Isabelle Dacquignies, Halil Koc, and Martin Eberle . Find more information about Crossref citation counts. Information. New Heteroaromatic Azo Compounds Based on Pyridine, Isoxazole, and Benzothiazole for Efficient and Highly Selective Amidation and Mono- Aerobic Oxidative Amidation of Aromatic and Cinnamic Aldehydes with Secondary Amines by CuI/2-Pyridonate Catalytic System. You have to login with your ACS ID befor you can login with your Mendeley account. The well-known Copper-free Azide-Phosphine reaction (Staudinger Ligation) lity of is hampered by the instabi phosphines and slow reaction kinetics. Rolf Kleineweischede, Christian P. R. Hackenberger. Mechanism of Amide Bond Formation from Carboxylic Acids and Amines Promoted by 9-Silafluorenyl Dichloride Derivatives. http://pubs.acs.org/page/copyright/permissions.html, https://doi.org/10.1021/acs.chemrev.9b00665, https://doi.org/10.1021/acs.chemrev.8b00657, https://doi.org/10.1021/acs.orglett.7b01132, https://doi.org/10.1021/acs.chemrev.6b00237, https://doi.org/10.1021/acs.biomac.5b00855, https://doi.org/10.1002/0471264180.or097.02, https://doi.org/10.1016/j.tetlet.2018.08.026, https://doi.org/10.1007/s11426-017-9056-5, https://doi.org/10.1016/B978-0-323-50878-0.00002-1, https://doi.org/10.1002/9783527683451.ch4, https://doi.org/10.1002/9783527800599.ch5, https://doi.org/10.1007/978-1-4939-2020-4_4, https://doi.org/10.1016/j.dyepig.2013.07.010, https://doi.org/10.1016/j.bmc.2013.02.045, https://doi.org/10.3390/molecules18044373, https://doi.org/10.1002/9781118526996.ch4, https://doi.org/10.1016/B978-0-12-382239-0.00036-4, https://doi.org/10.1016/j.tet.2012.08.059, https://doi.org/10.1002/9780470638859.conrr595, https://doi.org/10.1016/j.bmc.2010.07.018, https://doi.org/10.1016/j.bmcl.2010.05.106, https://doi.org/10.1002/047084289X.rn01051, https://doi.org/10.1016/j.bmc.2008.02.047, https://doi.org/10.1016/S0076-6879(09)62002-4, https://doi.org/10.1002/9780470048672.wecb635, https://doi.org/10.1016/B978-0-12-370501-3.00031-X, https://doi.org/10.1007/978-1-60327-375-6_32, https://doi.org/10.1002/9780470842898.rn00731, https://doi.org/10.1002/9780471264194.fos04781, https://doi.org/10.1016/j.tet.2006.09.045, https://doi.org/10.1016/j.tet.2005.08.031, https://doi.org/10.1146/annurev.biophys.34.040204.144700, https://doi.org/10.1111/j.1399-3011.2005.00241.x, https://doi.org/10.1111/j.1399-3011.2005.00214.x, https://doi.org/10.1016/B0-08-044655-8/00095-7, https://doi.org/10.1016/S0040-4039(03)01014-1, https://doi.org/10.1007/978-94-007-0958-4_27. A type of novel fluorescent phosphinimine derivative: Catalyst-free simple synthesis and optical properties. This article is cited by Files available from the ACS website may be downloaded for personal use only. Fax: (608) 262-3453. Andrew D. Kosal, Erin E. Wilson, Brandon L. Ashfeld. Hosahalli P. Hemantha, Narasimhamurthy Narendra, Vommina V. Sureshbabu. Rijkers, Johan Kemmink, Rob M.J. Liskamp. All Rights Reserved. The reaction between an azide and a phosphine forming an aza-ylide was first reported in 1919 by Nobel Prize laureate Herrmann Staudinger. These metrics are regularly updated to reflect usage leading up to the last few days. Intramolecular Staudinger Ligation: A Powerful Ring-Closure Method To Form Medium-Sized Lactams. Protein Assembly by Orthogonal Chemical Ligation Methods. Conjugation Chemistry Principles and Surface Functionalization of Nanomaterials. When working with live cells these reactions offer the advantage of not having the cytotoxicity associated with Cu-catalyzed cycloadditions. Cu-free cycloadditions offer efficient ligation reactions useful for a variety of bioconjugation applications. It has found widespread application in chemical synthesis, and is valuable as a highly chemoselective ligation method for the preparation of bioconjugates. Hackenberger. Type in Product Names, Product Numbers, or CAS Numbers to see suggestions. Jeet Kalia,, Nicholas L. Abbott, and.
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