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Aureggi, Valentina, Sedelmeier, Gottfried (2007) 1,3-Dipolar Cycloaddition: Click Chemistry for the Synthesis of 5-Substituted Tetrazoles from Organoaluminum Azides and Nitriles. Angewandte Chemie International Edition, 46 (44). 8440-8444 doi:10.1002/anie.200701045

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Reference TypeJournal (article/letter/editorial)
Title1,3-Dipolar Cycloaddition: Click Chemistry for the Synthesis of 5-Substituted Tetrazoles from Organoaluminum Azides and Nitriles
JournalAngewandte Chemie International Edition
AuthorsAureggi, ValentinaAuthor
Sedelmeier, GottfriedAuthor
Year2007 (November 12)Volume46
Issue44
PublisherWiley
DOIdoi:10.1002/anie.200701045Search in ResearchGate
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Mindat Ref. ID8582844Long-form Identifiermindat:1:5:8582844:3
GUID0
Full ReferenceAureggi, Valentina, Sedelmeier, Gottfried (2007) 1,3-Dipolar Cycloaddition: Click Chemistry for the Synthesis of 5-Substituted Tetrazoles from Organoaluminum Azides and Nitriles. Angewandte Chemie International Edition, 46 (44). 8440-8444 doi:10.1002/anie.200701045
Plain TextAureggi, Valentina, Sedelmeier, Gottfried (2007) 1,3-Dipolar Cycloaddition: Click Chemistry for the Synthesis of 5-Substituted Tetrazoles from Organoaluminum Azides and Nitriles. Angewandte Chemie International Edition, 46 (44). 8440-8444 doi:10.1002/anie.200701045
In(2007, November) Angewandte Chemie International Edition Vol. 46 (44) Wiley

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Aureggi, Valentina, Sedelmeier, Gottfried (2007) 1,3-Dipolar Cycloaddition: Click Chemistry for the Synthesis of 5-Substituted Tetrazoles from Organoaluminum Azides and Nitriles. Angewandte Chemie, 119 (44). 8592-8596 doi:10.1002/ange.200701045
Bosch, LluĂ­s, Vilarrasa, Jaume (2007) Cu2(OTf)2-Catalyzed and Microwave-Controlled Preparation of Tetrazoles from Nitriles and Organic Azides under Mild, Safe Conditions. Angewandte Chemie International Edition, 46 (21). 3926-3930 doi:10.1002/anie.200605095
Lutz, Jean-François (2007) 1,3-Dipolar Cycloadditions of Azides and Alkynes: A Universal Ligation Tool in Polymer and Materials Science. Angewandte Chemie International Edition, 46 (7). 1018-1025 doi:10.1002/anie.200604050
Jin, Tienan, Yamamoto, Yoshinori (2007) An Efficient, Facile, and General Synthesis of 1H-Indazoles by 1,3-Dipolar Cycloaddition of Arynes with Diazomethane Derivatives. Angewandte Chemie International Edition, 46 (18). 3323-3325 doi:10.1002/anie.200700101
LĂłpez-PĂ©rez, Ana, Robles-MachĂ­n, RocĂ­o, Adrio, Javier, Carretero, Juan Carlos (2007) Oligopyrrole Synthesis by 1,3-Dipolar Cycloaddition of Azomethine Ylides with Bissulfonyl Ethylenes. Angewandte Chemie International Edition, 46 (48). 9261-9264 doi:10.1002/anie.200703258
Zeng, Linwei, Li, Jiaming, Cui, Sunliang (2022) Rhodium‐Catalyzed Atroposelective Click Cycloaddition of Azides and Alkynes. Angewandte Chemie International Edition, 61 (28) doi:10.1002/anie.202205037
Nåjera, Carmen, Sansano, José M. (2005) Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides and Alkenes: The Direct Strategy To Prepare Enantioenriched Highly Substituted Proline Derivatives. Angewandte Chemie International Edition, 44 (39). 6272-6276 doi:10.1002/anie.200501074
Erhard, Thomas, Ehrlich, Gunnar, Metz, Peter (2011) A Total Synthesis of (±)-Codeine by 1,3-Dipolar Cycloaddition. Angewandte Chemie International Edition, 50 (17). 3892-3894 doi:10.1002/anie.201007448
Demko, Zachary P., Sharpless, K. Barry (2002) A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Acyltetrazoles from Azides and Acyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support. Angewandte Chemie International Edition, 41 (12). 2113pp. doi:10.1002/1521-3773(20020617)41:12<2113::aid-anie2113>3.0.co;2-q
Demko, Zachary P., Sharpless, K. Barry (2002) A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Sulfonyl Tetrazoles from Azides and Sulfonyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support. Dedicated to Professor Rolf Huisgen, the pioneer of this large and extremely useful family of reactions. Angewandte Chemie International Edition, 41 (12). 2110pp. doi:10.1002/1521-3773(20020617)41:12<2110::aid-anie2110>3.0.co;2-7
Gutmann, Bernhard, Roduit, Jean-Paul, Roberge, Dominique, Kappe, C. Oliver (2010) Synthesis of 5-Substituted 1H-Tetrazoles from Nitriles and Hydrazoic Acid by Using a Safe and Scalable High-Temperature Microreactor Approach. Angewandte Chemie International Edition, 49 (39). 7101-7105 doi:10.1002/anie.201003733
 
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