biblio
“Total synthesis of twelve membered resorcyclic acid lactones, (R)-penicimenolide A, (R)-resorcyclide and (R)-dihydroresorcyclide”, Tetrahedron, vol. 85, p. 132059, 2021.
, “Specific stereoisomeric conformations determine the drug potency of cladosporin scaffold against malarial parasite”, Journal of Medicinal Chemistry, vol. 61, no. 13, pp. 5664-5678, 2018.
, “Scalable synthesis of cladosporin”, Tetrahedron Letters, vol. 60, no. 12, pp. 831-833, 2019.
, “Ready access to benzannulated [5,5]-oxaspirolactones using Au(III)-catalyzed cascade cyclizations”, Journal of Organic Chemistry, vol. 87, no. 5, pp. 3025-3041, 2022.
, “Herbicidal bio-assay of isocladosporin enantiomers and determination of its plausible absolute configuration”, Journal of Antibiotics, vol. 74, no. 4, pp. 280-284, 2021.
, “DFT/NMR approach for the configuration assignment of groups of stereoisomers by the combination and comparison of experimental and predicted sets of data”, Journal of Organic Chemistry, vol. 85, no. 5, pp. 3297-3306, 2020.
, “Design, synthesis, and structural analysis of cladosporin-based inhibitors of malaria parasites”, ACS Infectious Diseases, vol. 7, no. 6, pp. 1777–1794, 2021.
, “Biological process of lysine-tRNA charging is therapeutically targetable in liver cancer”, Liver International, vol. 41, no. 1, pp. 206-219, 2021.
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