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Synfacts 2011(11): 1206-1206
DOI: 10.1055/s-0031-1289214
DOI: 10.1055/s-0031-1289214
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Iridium-Catalyzed Asymmetric Allylations
A. Hassan, I. A. Townsend, M. J. Krische*
University of Texas at Austin, USA
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
19. Oktober 2011 (online)

Significance
The Grignard Nozaki-Hiyama allylation of aldehydes is one of the most straightforward means to construct homoallylic alcohols. There has been a concerted effort by the synthetic community to provide asymmetric variants of this transformation. The Krische group has demonstrated that transfer hydrogenation is a versatile means to apply alcohols (as precursors to aldehydes) and π-unsaturated reactants in enantioselective allylations. It is remarkable that electrophiles in the alcohol oxidation state can be utilized without the necessity of stoichiometric metal reductants.