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Ruthenium-Catalyzed Organic Synthesis in Aqueous Media

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Ruthenium Catalysts and Fine Chemistry

Part of the book series: Topics in Organometallic Chemistry ((TOPORGAN,volume 11))

Abstract

Ruthenium-catalyzed organic synthesis in aqueous media has attracted much attention recently. The applications of ruthenium in aqueous media are generally in atom-economical and environmentally benign reactions. In this review, our focus is on ruthenium-catalyzed C–C bond formations. Ruthenium-catalyzed activation of the C–H bond of allyl alcohol and tandem isomerization/aldol reaction are discussed. Also, through activation of the C–H bond of terminal alkynes, direct additions of alkynes to aldehydes and imines to give Grignard-type reaction products were realized in aqueous media. Various ruthenium-catalyzed nonmetathesis C–C formations in aqueous media, most of which were on the addition to alkynes, provided useful methodology for organic synthesis. In addition, ruthenium-catalyzed ring-closing metathesis and ring-opening metathesis polymerization reactions in water are briefly overviewed.

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Correspondence to Chao-Jun Li .

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Christian Bruneau Pierre H. Dixneuf

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© 2004 Springer-Verlag

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Wang, M., Li, CJ. (2004 ). Ruthenium-Catalyzed Organic Synthesis in Aqueous Media. In: Bruneau, C., Dixneuf, P.H. (eds) Ruthenium Catalysts and Fine Chemistry. Topics in Organometallic Chemistry, vol 11. Springer, Berlin, Heidelberg. https://doi.org/10.1007/b94648

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  • DOI: https://doi.org/10.1007/b94648

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  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-20543-2

  • Online ISBN: 978-3-540-40027-1

  • eBook Packages: Springer Book Archive

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