Title: A Very Simple Copper‐Catalyzed Synthesis of Anilines by Employing Aqueous Ammonia
Abstract: Angewandte Chemie International EditionVolume 48, Issue 2 p. 337-339 Communication A Very Simple Copper-Catalyzed Synthesis of Anilines by Employing Aqueous Ammonia† Ning Xia, Ning Xia CNRS, UMR 5253, Institut Charles Gerhardt Montpellier AM2N, ENSCMontpellier, 8, rue de l'Ecole Normale, 34296 Montpellier Cedex 5 (France), Fax: (+33) 467-144-319Search for more papers by this authorMarc Taillefer Dr., Marc Taillefer Dr. [email protected] CNRS, UMR 5253, Institut Charles Gerhardt Montpellier AM2N, ENSCMontpellier, 8, rue de l'Ecole Normale, 34296 Montpellier Cedex 5 (France), Fax: (+33) 467-144-319Search for more papers by this author Ning Xia, Ning Xia CNRS, UMR 5253, Institut Charles Gerhardt Montpellier AM2N, ENSCMontpellier, 8, rue de l'Ecole Normale, 34296 Montpellier Cedex 5 (France), Fax: (+33) 467-144-319Search for more papers by this authorMarc Taillefer Dr., Marc Taillefer Dr. [email protected] CNRS, UMR 5253, Institut Charles Gerhardt Montpellier AM2N, ENSCMontpellier, 8, rue de l'Ecole Normale, 34296 Montpellier Cedex 5 (France), Fax: (+33) 467-144-319Search for more papers by this author First published: 22 December 2008 https://doi.org/10.1002/anie.200802569Citations: 231 † We are grateful to the CNRS and the region of Languedoc Roussillon for a PhD grant and financial support. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Graphical Abstract Phasing up to matters: The use of aqueous ammonia in a biphasic system with a copper catalyst and diketone supporting ligands allows the catalytic amination of both activated and unactivated aryl and heteroaryl iodides and bromides under very mild conditions (see scheme; R=electron-donating or -withdrawing group; acac=acetylacetonate). Citing Literature Supporting Information Detailed facts of importance to specialist readers are published as "Supporting Information". Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Filename Description anie_200802569_sm_miscellaneous_information.pdf621 KB miscellaneous information Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article. Volume48, Issue2January 2, 2009Pages 337-339 RelatedInformation
Publication Year: 2008
Publication Date: 2008-12-22
Language: en
Type: article
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 252
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