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 2005(3): 0339-0339
DOI: 10.1055/s-2005-921638
DOI: 10.1055/s-2005-921638
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York
Pd-Catalyzed Coupling of Propargylic Oxiranes with Arylboronic Acids
M. Yoshida*, H. Ueda, M. Ihara*
University of Tokushima, and Tohoku University, Sendai, Japan
Further Information
Publication History
Publication Date:
22 November 2005 (online)
Significance
Allenols are widely represented among natural products and also are useful synthetic intermediates. The usual approach to this class of compounds is the reaction of propargylic oxiranes with organometallic reagents. The described method allows the use of stable and often commercially available arylboronic acids instead of organometallic reagents for the synthesis of substituted 2,3-allenols. The starting oxiranes are readily prepared by epoxidation of enynes. For chiral substrates the method of Shi et al. can be used.