biblio
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, “Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: an effective strategy towards development of potent anti-tubercular agents”, European Journal of Medicinal Chemistry, vol. 259, p. 115633, 2023.
, “Route to benzimidazol-2-ones via decarbonylative ring contraction of quinoxalinediones: application to the synthesis of flibanserin, A drug for treating hypoactive sexual desire disorder in women and marine natural product hunanamycin analogue”, ACS Omega, vol. 2 , no. 8, pp. 5137-5141, 2017.
, “Repurposing of a drug scaffold: identification of novel sila analogues of rimonabant as potent antitubercular agents”, European Journal of Medicinal Chemistry, vol. 122, pp. 723-730, 2016.
, “Multi-gram scale synthesis of hunanamycin A, an antibiotic natural product from the marine source”, Tetrahedron Letters, vol. 57, no. 32, pp. 3662-3663, 2016.
, “Identification of new modulator of DNA repairing pathways based on natural product (±)-peharmaline A”, Bioorganic & Medicinal Chemistry, vol. 91, p. 117365, 2023.
, “General approach to N-heterocyclic carbenes with a fused tetracyclic core: ligands for suzuki-miyaura cross-coupling reaction”, European Journal of Organic Chemistry, no. 21, pp. 4482-4486, 2014.
, “First total synthesis of hunanamycin A”, Organic Letters, vol. 15, no. 17, pp. 4556-4559, 2013.
, “Antibiotic natural product hunanamycin A: Lead identification towards anti-Salmonella agents”, European Journal of Medicinal Chemistry, vol. 236, p. 114245, 2022.