Asymmetric Organocatalysis

As nucleophiles, simple alkenes are typically so unreactive that only highly active electrophiles, such as carbocations, peroxides, and halogens will react with them. For the generation of carbon-carbon bonds, milder methods will often be required. Fortunately, it is possible to increase the reactiv...

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Bibliographische Detailangaben
Weitere Verfasser: List, Benjamin (HerausgeberIn)
Format: Livre numérique
Sprache:Anglais
Veröffentlicht: Berlin, Heidelberg : Springer Berlin Heidelberg 2009.
Schriftenreihe:Topics in Current Chemistry 291
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Edition sous un autre format:• Asymmetric organocatalysis, [éd. par] Benjamin List, Heidelberg, Springer Verlag, 2009, 1 vol. (X-460 p.), Topics in current chemistry, 978-3-642-02814-4
Inhaltsangabe:
  • Kerstin Etzenbach-Effers, Albrecht Berkessel: Non-Covalent Organocatalysis Based on Hydrogen Bonding: Elucidation of Reaction Paths by Computational Methods Petri M. Pihko, Inkeri Majander, and Anniina Erkkilä: Enamine Catalysis Jennifer L. Moore, Tomislav Rovis: Lewis Base Catalysts 6: Carbene Catalysts Amal Ting, Jennifer M. Goss, Nolan T. McDougal, and Scott E. Schaus: Brùnsted Base Catalysts O. Andrea Wong, Yian Shi: Chiral Ketone and Iminium Catalysts for Olefin Epoxidation Alan C. Spivey, Stellios Arseniyadis: Amine, Alcohol and Phosphine Catalysts for Acyl Transfer Reactions John B. Brazier, Nicholas C.O. Tomkinson: Lewis Base Catalysts 2 Secondary and Primary Amine Catalysts for Iminium Catalysis Oksana Sereda, Sobia Tabassum, and René Wilhelm: Lewis Acid Organocatalysts Daniela Kampen, Corinna M. Reisinger, and Benjamin List: Chiral Bronsted Acids for C Organocatalysis