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      • Record: found
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      Amines as key building blocks in Pd-assisted multicomponent processes

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          Summary

          In the last few years, palladium-mediated three-component synthesis has emerged as an important synthetic methodology to gain access to nitrogen-containing structures. The latest developments in this area are discussed in this review.

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          Synthesis and functionalization of indoles through palladium-catalyzed reactions.

          Sandro Cacchi, Giancarlo Fabrizi, Pilar Hoyos (2005)
          Article 0 comments Cited 237 times – based on 0 reviews     Review now
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            Palladium-catalyzed aminosulfonylation of aryl halides.

            Bao Kim Nguyen, Edward Emmett, Michael C. Willis (2010)
            The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to deliver aryl N-aminosulfonamides is described. The colorless crystalline solid DABCO·(SO(2))(2) was used as a convenient source of sulfur dioxide. The reaction tolerates significant variation of both the aryl iodide and hydrazine coupling partners.
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              One-pot construction of pyrazoles and isoxazoles with palladium-catalyzed four-component coupling.

              Trevor Mori, A. Ahmed, Kei Kobayashi (2005)
              [reaction: see text] Four-component coupling of a terminal alkyne, hydrazine (hydroxylamine), carbon monoxide, and an aryl iodide furnishes pyrazole or isoxazole derivatives in the presence of a palladium catalyst. The reaction proceeds at room temperature and an ambient pressure of carbon monoxide in an aqueous solvent system.
              Article 0 comments Cited 28 times – based on 0 reviews     Review now
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                Author and article information

                Contributors
                Didier Bouyssi
                Nuno Monteiro
                Geneviève Balme
                Thomas J J Müller: Role: Guest Editor
                Journal
                Journal ID (nlm-ta): Beilstein J Org Chem
                Title: Beilstein Journal of Organic Chemistry
                Publisher: Beilstein-Institut (Trakehner Str. 7-9, 60487 Frankfurt am Main, Germany )
                ISSN (Electronic): 1860-5397
                Publication date Collection: 2011
                Publication date (Electronic): 10 October 2011
                Volume: 7
                Pages: 1387-1406
                Affiliations
                [1 ]ICBMS, Institut de Chimie et Biochimie Moléculaire et Supramoléculaire, CNRS UMR 5246, Université Lyon 1, ESCPE Lyon. 43, Bd du 11 Novembre 1918, 69622, Villeurbanne, France
                Article
                DOI: 10.3762/bjoc.7.163
                PMC ID: 3201053
                PubMed ID: 22043250
                SO-VID: fb5b8d94-9bb8-4a59-82ad-0755d4ea9f19
                Copyright © Copyright © 2011, Bouyssi et al; licensee Beilstein-Institut.
                License:

                This is an Open Access article under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: ( http://www.beilstein-journals.org/bjoc)

                History
                Date received : 20 May 2011
                Date accepted : 14 September 2011
                Categories
                Subject: Review
                Subject: Chemistry
                Subject: Organic Chemistry

                ScienceOpen disciplines: Organic & Biomolecular chemistry
                Keywords: amines,multicomponent reactions,palladium
                Data availability:
                ScienceOpen disciplines: Organic & Biomolecular chemistry
                Keywords: amines, multicomponent reactions, palladium

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