Addition of Cyanoethyl Groups to Ring a of Triterpenoids

@article{Galaiko2018AdditionOC,
  title={Addition of Cyanoethyl Groups to Ring a of Triterpenoids},
  author={N. V. Galaiko and I. A. Tolmacheva and E. V. Igosheva and O. Savinova and V. V. Grishko},
  journal={Chemistry of Natural Compounds},
  year={2018},
  volume={54},
  pages={305-309}
}
The potential for cyanoethylation of ring A of triterpenoids and their A-seco derivatives prepared from allobetulone and methyl betulonate was investigated. Triterpenoids with a cyanoethyl moiety on C-1, C-2, and C-3 and derivatives with two cyanoethyl groups on ring A were synthesized. The inhibitory activity of the synthesized compounds for herpes simplex virus type 1 was studied in vitro. 

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