Biosynthesis of swainsonine in the diablo locoweed (Astragalus oxyphyrus)

Tetrahedron Letters
1988.0

Abstract

In addition to the toxic indolizidine alkaloid swainsonine, the diablo locoweed (Astragalu oxyphysus) has been found to produce [1,8a-trans]-1-hydroxyindolizidine and [1,8a-trans-1,2-cis]-1,2-dihydroxyindolizidine, known precursors of swainsonine in the fungus Rhizoctonia leguminicola. As in the fungus, [G-3H]-pipecolic acid is incorporated into all three alkaloids. It is proposed that swainsonine biosynthesis in A. oxyphysus occurs by a pathway very similar to the fungal route. © 1988.

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