Article ID Journal Published Year Pages File Type
5288802 Tetrahedron Letters 2006 4 Pages PDF
Abstract
A short and efficient two-step synthesis of the antimalarial robustadials A and B via a key biomimetic three-component reaction, which involves in situ generation of an o-quinone methide via Knoevenagel condensation and subsequent Diels-Alder cycloaddition with (−)-β-pinene is described.
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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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A two-step biomimetic synthesis of antimalarial robustadials A and B
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