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Birch Reaction Followed by Asymmetric Iridium-Catalysed Hydrogenation
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry.
2011 (English)In: Synthesis (Stuttgart), ISSN 0039-7881, E-ISSN 1437-210X, no 23, p. 3796-3800Article in journal (Refereed) Published
Abstract [en]

Birch reaction products are asymmetrically hydrogenated with high enantio- and diastereoselectivity via iridium catalysts. This new method of producing chiral compounds was explored for a variety of 1,3-di- and 1,2,4-tri-substituted cyclohexadienes.

Place, publisher, year, edition, pages
2011. no 23, p. 3796-3800
Keyword [en]
asymmetric catalysis, iridium, hydrogenation, reduction, radical reaction
National Category
Natural Sciences
Identifiers
URN: urn:nbn:se:uu:diva-167652DOI: 10.1055/s-0031-1289569ISI: 000298156900007OAI: oai:DiVA.org:uu-167652DiVA: diva2:488291
Available from: 2012-02-01 Created: 2012-01-31 Last updated: 2017-12-08Bibliographically approved

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Cadu, AlbanPaptchikhine, AlexanderAndersson, Pher G.

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