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説明
A stereoselective synthetic route to Nuphar quinolizidine alkaloid, (−)-deoxynupharidine, was established by employing reductive carbon–nitrogen bond cleavage, followed by simultaneous recyclization of a proline derivative with samarium diiodide, and an intramolecular ring-closing metathesis, as the key steps.
収録刊行物
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- Tetrahedron Letters
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Tetrahedron Letters 46 5161-5163, 2005-08-01
Elsevier BV
