Partial Synthesis of Crassicauline A from Yunaconitine
- PMID: 32297141
- PMCID: PMC7176785
- DOI: 10.1007/s13659-020-00238-0
Partial Synthesis of Crassicauline A from Yunaconitine
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.
Keywords: Crassicauline A; Diterpenoid alkaloids; Yunaconitine.
Conflict of interest statement
The authors declare no conflict of interest.
References
-
- Chen SY. Acta Chem. Sin. 1979;37:15–20.
-
- Wu C. J. Xinjiang Med. Univ. 2011;34:1153–1157.
-
- Zhang HB, Hu WY, Li L, Dai XT, Zhang DZ. China. Patent. 1991;1054976:2.
-
- Zhang RP, Chen SY, Zhou J. Acta Bot. Yunnanica Plant Divers. 1998;20:474–478.
-
- Tang XC, Liu XJ, Lu WH. Acta Pharm. Sin. 1986;21:886. - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous
