Title of article
Asymmetric synthesis of (−)-codonopsinine
Author/Authors
Davies، نويسنده , , Stephen G. and Lee، نويسنده , , James A. and Roberts، نويسنده , , Paul M. and Thomson، نويسنده , , James E. and West، نويسنده , , Callum J.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2011
Pages
4
From page
6477
To page
6480
Abstract
The asymmetric synthesis of (−)-codonopsinine was achieved in 7 steps (from commercially available tert-butyl crotonate) in 5% overall yield and >99:1 dr. The key step in this synthesis involved ring-closing iodoamination of a functionalised homoallylic amine, which occurred with concomitant N-debenzylation, to give a 3-iodopyrrolidine that was elaborated to (−)-codonopsinine.
Keywords
(?)-Codonopsinine , Ring-closing iodoamination , pyrrolidine , Lithium amide
Journal title
Tetrahedron Letters
Serial Year
2011
Journal title
Tetrahedron Letters
Record number
1879634
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