File:Sherburn's Total Synthesis of (-)-Artigenin.png
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Sherburn's Total Synthesis of (-)-Arctigenin
The following synthesis begins at the top left and follows the respective arrows to the bottom left product, (-)-Arctigenin.
The first step involves the formation of the boron enolate of the oxazolidinone (right structure), which then is reacted with the given aldehyde(left) to produce this first structure in an approximate 92% yield.
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current | 11:55, 19 May 2010 | 2,145 × 3,108 (131 KB) | Terpstra (talk | contribs) | ||
13:31, 15 May 2010 | 504 × 799 (25 KB) | Terpstra (talk | contribs) | Sherburn's Total SYnthesis of (-)-Arctigenin |
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