C(sp3)-H Arylation of Pentacyclic Triterpenoids
13th Paul Walden Symposium on Organic Chemistry: Program and Abstract Book 2023
Vladislavs Kroškins

Naturally abundant pentacyclic triterpenoids are significant secondary metabolites which have aroused huge interest by possessing wide range of remarkable biological activities such as antitumor,1 antidiabetic,2 anti-inflammatory3 and antiviral activities4. Oleanolic, ursolic acids and betulin, are the most recognizable compounds of this branch, which are isolated from various plants. The aim of this work is to obtain novel triterpenoic derivatives by C-H arylation at C(22). For this purpose, precursors bearing picolinic amide directing groups were synthesized.


Atslēgas vārdi
C-H activation, pentacyclic triterpenoids
Hipersaite
https://walden.osi.lv/wp-content/uploads/2023/09/Abstract_book_Walden_2023.pdf

Kroškins, V. C(sp3)-H Arylation of Pentacyclic Triterpenoids. No: 13th Paul Walden Symposium on Organic Chemistry: Program and Abstract Book, Latvija, Riga, 14.-15. septembris, 2023. Riga: OSI, 2023, 46.-46.lpp.

Publikācijas valoda
English (en)
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