Highly Stereoselective [4 + 3] Cycloadditions of Nitrogen-Stabilized Oxyallyl Cations with Pyrroles. An Approach to Parvineostemonine
Author:
Affiliation:
1. Division of Pharmaceutical Sciences and Department of Chemistry, University of Wisconsin, Madison, Rennebohm Hall, 777 Highland Avenue, Madison, Wisconsin 53705
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol070103n
Reference33 articles.
1. Asymmetric Catalytic [4+3] Cycloaddition Reactions
2. On the Inherent Instability of α-Amino α‘-Fluoro Ketones. Evidence for Their Transformation to Reactive Oxyvinyliminium Ion Intermediates
3. The [4 + 3]-Cycloaddition/Quasi-Favorskii Process. Synthesis of the Carbocyclic Core of Tricycloclavulone
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