Title of article
First total synthesis of (+)-viroallosecurinine
Author/Authors
Honda، نويسنده , , Toshio and Namiki، نويسنده , , Hidenori and Watanabe، نويسنده , , Masayuki and Mizutani، نويسنده , , Hirotake، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
3
From page
5211
To page
5213
Abstract
The first diastereoselective chiral synthesis of (+)-viroallosecurinine, isolated from Securinega virosa as a cytotoxic alkaloid, was achieved by using a chelation-controlled addition of an alkyne moiety to the corresponding ketone, and a ring-closing metathesis, as key reactions.
Keywords
Chelation-controlled addition , Securinega alkaloid , Diastereoselective total synthesis , (+)-Viroallosecurinine , Ring closing-metathesis
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1842281
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