| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5282534 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A novel and stereocontrolled synthetic path to a coccinellid alkaloid, (â)-adalinine, was established by employing the reductive carbon-nitrogen bond cleavage reaction and subsequent recyclization of a 3-oxopyrrolidine derivative with samarium diiodide, as key steps, where water was found to be the best proton source.
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Authors
Toshio Honda, Chihiro Hisa,