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Synfacts 2010(5): 0558-0558
DOI: 10.1055/s-0029-1219641
DOI: 10.1055/s-0029-1219641
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Enantioenriched Allenes from 1,1-Cyclopropanediesters
P. Cérat, P. J. Gritsch, S. R. Goudreau, A. B. Charette*
Université de Montréal, Canada
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
22. April 2010 (online)
Significance
In this paper the authors report a protocol allowing the formation of chiral allenes via SN2′ addition of organocuprates to enantioenriched propargylcyclopropanes. Development of such a method is important in light of high synthetic utility of chiral allenes, which lacked an expedient synthetic approach thus far despite a number of reports. Under optimized conditions, a range of 1,7-addition products was obtained with 78-89% yields. Complete preservation of enantiomeric purity was observed for an enantioenriched substrate 1, leading to a synthetic precursor of a pheromone 2 of Acanthoscelides obtectus.