| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266207 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The asymmetric synthesis of (â)-codonopsinine was achieved via ring-closing iodoamination of a functionalised homoallylic amine, followed by functional group manipulation of the resultant 3-iodopyrrolidine.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Stephen G. Davies, James A. Lee, Paul M. Roberts, James E. Thomson, Callum J. West,