Highly stereoselective [4 + 3] cycloadditions of nitrogen-stabilized oxyallyl cations with pyrroles: an approach to parvineostemonine.

Org Lett

Division of Pharmaceutical Sciences and Department of Chemistry, University of Wisconsin, Madison, Rennebohm Hall, Madison, WI 53705, USA.

Published: March 2007

[structure: see text]. A highly stereoselective [4 + 3] cycloaddition of N-substituted pyrroles with allenamide-derived nitrogen-stabilized chiral oxyallyl cations is described here. This method provides an approach for constructing tropinone alkaloids.

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http://dx.doi.org/10.1021/ol070103nDOI Listing

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