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(5): 0525-0525
DOI: 10.1055/s-0030-1259827
DOI: 10.1055/s-0030-1259827
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Enantioselective Cyclopropenation of Alkynes
X. Cui, X. Xu, H. Lu, S. Zhu, L. Wojtas, X. P. Zhang*
University of South Florida, Tampa, USA
Further Information
Publication History
Publication Date:
15 April 2011 (online)
Significance
Chiral cyclopropenes are highly strained carbocyclic compounds with unique properties that make them desirable synthons for a variety of synthetic transformations. The authors report a chiral metalloradical catalyst for a highly enantioselective cyclopropenation of terminal conjugated alkynes (specifically terminal aromatic or 1,3-enynes) using α-cyanodiazoacetamides and α-cyanodiazoacetates. The authors comment on the radical nature of the reaction mechanism based on the reactivity profile and the chemoselectivity observed.