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  1. 1.   Sesquiterpene Coumarin Ethers and Phenylpropanoids from the Roots of Ferula drudeana, the Putative Anatolian Ecotype of the Silphion Plant
  2. Kuran, Fadil Kaan; Senadeera, Sarath P D; Wang,Dongdong; Hwang,Jiyeon; Goncharova,Ekaterina; Wilson,Jennifer; Wamiru, Antony; Wilson,Brice; Pruett, Nathanael; Du,Lin; Hoang, Chuong D; Beutler,John; Miski, Mahmut
  3. Molecules (Basel, Switzerland). 2025, Apr 25; 30(9): 1916.
  1. 2.   Novel Cytotoxic Sesquiterpene Coumarin Ethers and Sulfur-Containing Compounds from the Roots of Ferula turcica
  2. Eruçar, Fatma Memnune; Senadeera, Sarath P D; Wilson,Jennifer; Goncharova,Katya; Beutler,John; Miski, Mahmut
  3. Molecules (Basel, Switzerland). 2023, Jul 28; 28(15):
  1. 3.   Evolution of the total syntheses of ustiloxin natural products and their analogues
  2. Li, P. X.; Evans, C. D.; Wu, Y. Z.; Cao, B.; Hamel, E.; Joullie, M. M.
  3. Journal of the American Chemical Society. 2008 130(7): 2351-2364.
  1. 4.   Antitumo agents 238. Anti-tubulin and in vitro cytotoxic effects of N-substituted allocolchicinoids
  2. Nakagawa-Goto, K.; Jung, M. K.; Hamel, E.; Wu, C. C.; Bastow, K. F.; Brossi, A.; Ohta, S.; Lee, K. H.
  3. Heterocycles. 2005 65(3): 541-550.
  1. 5.   Enantioselective synthesis of (S)-3-carboxy-4-((carboxy)difluoromethyl)phenylalanine in protected form and its incorporation into a PTP-1B-directed tripeptide
  2. Kang, S. U.; Yang, G.; Li, W.; Zhang, Z. Y.; Burke, T. R.
  3. Chemistry & Biodiversity. 2004 1(4): 626-633.
  1. 6.   Utilization of a peptide lead for the discovery of a novel PTP1M-binding motif
  2. Gao, Y.; Voigt, J.; Zhao, H.; Pais, G. C. G.; Zhang, X. C.; Wu, L.; Zhang, Z. Y.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2001 44(18): 2869-2878.
  1. 7.   First Synthesis of the Antimalarial Naphthylisoquinoline Alkaloid Dioncophylline C, and Its Unnatural Anti-Hiv Dimer, Jozimine C
  2. Bringmann, G.; Holenz, J.; Weirich, R.; Rubenacker, M.; Funke, C.; Boyd, M. R.; Gulakowski, R. J.; Francois, G.
  3. Tetrahedron. 1998 54(3-4): 497-512.
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