Natural Products and Bioprospecting (Apr 2020)

Partial Synthesis of Crassicauline A from Yunaconitine

  • Rong-Ping Zhang,
  • Yan-Jun Lin,
  • Hao-Fei Yu,
  • Si-Ying Chen,
  • Jun Zhou

DOI
https://doi.org/10.1007/s13659-020-00238-0
Journal volume & issue
Vol. 10, no. 2
pp. 105 – 108

Abstract

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Abstract Both Aconitum hemsleyanum and Aconitum geniculatun have abundant contents of yunaconitine (1). Yunaconitine (1) has similar skeleton to crassicauline A (3); the only difference between them is that 1 contains a α-hydroxyl group at C-3. Our team attempts to convert 1 into 3 because 3 owns pharmacological activity. There are two steps to achieve the transformation above: firstly, use dehydration reaction to transform yunaconitine (1) into dehydroyunaconitine (2); secondly, use hydrogen reduction to acquire crassicauline A (3). Compared with other methods, this one below is more suitable for production application and more concise; moreover, the cost is lower with higher yield. Graphic Abstract

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