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 2011(2): 0163-0163
DOI: 10.1055/s-0030-1259344
DOI: 10.1055/s-0030-1259344
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Stereoselective Iodocarbocyclization
A. Pradal, A. Nasr, P. Y. Toullec*, V. Michelet*
Chimie ParisTech, France
Further Information
Publication History
Publication Date:
19 January 2011 (online)
Significance
The authors report a diastereoselective iodocarbocyclization of 1,5-enynes to provide decorated cyclopentenes. With 1,5-enynes the 6-endo mode of cyclization has been previously observed and is more common; however, the authors have reversed this preference by judicious choice of substituents on the alkene moiety.