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  1. 1.   Synthesis of Fused Bicyclic Systems with Nitrogen Atom at the Bridgehead, Including Indolizidines and Quinolizidines
  2. Pepe, A.; Pamment, M.; Georg, G. I.; Malhotra, S. V.
  3. Journal of Organic Chemistry. 2011, May; 76(9): 3527-3530.
  1. 2.   Enhanced Stereoselectivity of a Cu(II) Complex Chiral Auxiliary in the Synthesis of Fmoc-L-gamma-carboxyglutamic Acid
  2. Smith, D. J.; Yap, G. P. A.; Kelley, J. A.; Schneider, J. P.
  3. Journal of Organic Chemistry. 2011, Mar; 76(6): 1513-1520.
  1. 3.   Preparation of orthogonally protected (2S,3R)-2-amino-3-methyl-4-phosphonobutyric acid (Pmab) as a phosphatase-stable phosphothreonine mimetic and its use in the synthesis of polo-box domain-binding peptides
  2. Liu, F.; Park, J. E.; Lee, K. S.; Burke, T. R.
  3. Tetrahedron. 2009 65(47): 9673-9679.
  1. 4.   Preparation of orthogonally-protected 3-methoxy-4-phosphonomethyl-L-phenylalanine, a new reagent for the synthesis of phosphotyrosyl mimetic-containing peptides
  2. Choi, W. J.; Xang, S. U.; Burke, T. R.
  3. Letters in Organic Chemistry. 2007, Sep; 4(6): 433-439.
  1. 5.   The triphosphate of beta-D-4 '-C-ethynyl-2 ',3 '-dideoxycytidine is the preferred enantiomer substrate for HIV reverse transcriptase
  2. Siddiqui, M. A.; Marquez, V. E.
  3. Bioorganic & Medicinal Chemistry. 2007, Jan; 15(1): 283-287.
  1. 6.   Neamphamide A, a new HIV-Inhibitory depsipeptide from the Papua New Guinea marine sponge Neamphius huxleyi
  2. Oku, N.; Gustafson, K. R.; Cartner, L. K.; Wilson, J. A.; Shigematsu, N.; Hess, S.; Pannell, L. K.; Boyd, M. R.; McMahon, J. B.
  3. Journal of Natural Products. 2004, AUG; 67(8): 1407-1411.
  1. 7.   Concise and enantioselective synthesis of Fmoc-Pmp(BUt)(2)-OH and design of potent Pmp-containing Grb2-SH2 domain antagonists
  2. Li, P.; Zhang, M. C.; Peach, M. L.; Liu, H. P.; Yang, D. J.; Roller, P. P.
  3. Organic Letters. 2003 5(17): 3095-3098.
  1. 8.   Asymmetric synthesis of a conformationally locked carboxylic analog of L-3 '-deoxythymine that mimics the South conformation: Biological implications and enzyme recognition
  2. Choi, Y. S.; Comin, M. J.; Clifford, G.; Balzarini, J.; Marquez, V. E.
  3. Abstracts of Papers of the American Chemical Society. 2003 225(Part 2): U195-U195.
  1. 9.   Design and synthesis of a beta-amino phosphotyrosyl mimetic suitably protected for peptide synthesis
  2. Lee, K.; Zhang, M. C.; Yang, D. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2002 12(23): 3399-3401.
  1. 10.   Synthesis of N-Fmoc 3-(4-(di-(tert- butyl)phosphonomethyl)phenyl)pipecolic acid as a conformationally constrained phosphotyrosyl mimetic suitably protected for peptide synthesis
  2. Liu, D. G.; Wang, X. Z.; Gao, Y.; Li, B. H.; Yang, D.; Burke, T. R.
  3. Tetrahedron. 2002 58(52): 10423-10428.
  1. 11.   Enantioselective synthesis of N-alpha-Fmoc protected (2S,3R)-3- phenylpipecolic acid. A constrained phenylalanine analogue suitably protected for solid-phase peptide synthesis
  2. Liu, D. G.; Gao, Y.; Wang, X. Z.; Kelley, J. A.; Burke, T. R.
  3. Journal of Organic Chemistry. 2002 67(5): 1448-1452.
  1. 12.   Antineoplastic agents 442. Synthesis and biological activities of dioxostatin
  2. Pettit, G. R.; Lippert, J. W.; Boyd, M. R.; Verdier-Pinard, P.; Hamel, E.
  3. Anti-Cancer Drug Design. 2000 15(5): 361-371.
  1. 13.   Antineoplastic agents 463. Synthesis of combretastatin A-3 diphosphate prodrugs
  2. Pettit, G. R.; Minardi, M. D.; Boyd, M. R.; Pettit, R. K.
  3. Anti-Cancer Drug Design. 2000 15(6): 397-403.
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