Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2009(9): 0992-0992
DOI: 10.1055/s-0029-1217624
DOI: 10.1055/s-0029-1217624
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of α-Hydroxyallenes by SN2′ of Propargylic Dioxolanones
X. Tang, S. Woodward*, N. Krause
The University of Nottingham, UK and Technische Universität Dortmund, Germany
Further Information
Publication History
Publication Date:
21 August 2009 (online)
Significance
This paper described a new catalytic method for the synthesis of α-hydroxyallenes by copper(I)-catalyzed SN2′ reaction of propargylic dioxolanones with Grignard reagents. A variety of primary and secondary α-hydroxyallenes were obtained with good to excellent yields via a highly anti-selective pathway. Moreover, this method could be applied to the synthesis of enantiomerically enriched allenes with complete chirality transfer.