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 2008(2): 0158-0158
DOI: 10.1055/s-2007-992451
DOI: 10.1055/s-2007-992451
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Stereoselective Conjugate Addition of 2,3-Allenoates with Grignard Reagents
Z. Lu, G. Chai, S. Ma*
Zhejiang University, Hangzhou and Shanghai Institute of Organic Chemistry, P. R. of China
Further Information
Publication History
Publication Date:
23 January 2008 (online)

Significance
The authors describe the regio- and stereoselective addition of Grignard reagents to 2,3-allenoates to generate β,γ-unsaturated esters. This reaction proceeds with less than 5 mol% of an iron catalyst and gives the esters in high yields. This is an important contribution to synthetic chemistry in that it uses an inexpensive iron catalyst and readily available Grignard reagents.