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(10): 1079-1079
DOI: 10.1055/s-0029-1217903
DOI: 10.1055/s-0029-1217903
Synthesis of Heterocycles
© Georg Thieme Verlag
Stuttgart ˙ New York
Stereoselective Synthesis of Spirooxindoles
R. Shintani*, S.-y. Hayashi, M. Murakami, M. Takeda, T. Hayashi*
Kyoto University, Japan
Further Information
Publication History
Publication Date:
22 September 2009 (online)
Significance
A stereoselective synthesis of spirooxindoles via decarboxylative cyclization of γ-methylidene-δ-valerolactones with N-methylisatins is described. Compared to ligand 1, the corresponding ligand 2 led to spirooxindoles with modest ee value and comparable yields and dr. The proposed mechanism indicates that the palladium-catalyzed decarboxylation of γ-methylidene-δ-valerolactones initiates the cyclization process and gives the target products.