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  1. 1.   SAVI, in silico generation of billions of easily synthesizable compounds through expert-system type rules
  2. Patel,Hitesh; Ihlenfeldt, Wolf-Dietrich; Judson, Philip N; Moroz, Yurii S; Pevzner, Yuri; Peach,Megan; Delannee,Victorien; Tarasova,Nadya; Nicklaus,Marc
  3. Scientific data. 2020, NOV 11; 7(1): 384.
  1. 2.   Samarium Iodide-Mediated Reformatsky Reactions for the Stereoselective Preparation of beta-Hydroxy-gamma-amino Acids: Synthesis of Isostatine and Dolaisoleucine
  2. Nelson, C. G.; Burke, T. R.
  3. Journal of Organic Chemistry. 2012, Jan; 77(1): 733-738.
  1. 3.   Microwave-Based Reaction Screening: Tandem Retro-Diels Alder/Diels-Alder Cycloadditions of o-Quinol Dimers
  2. Dong, S. W.; Cahill, K. J.; Kang, M. I.; Colburn, N. H.; Henrich, C. J.; Wilson, J. A.; Beutler, J. A.; Johnson, R. P.; Porco, J. A.
  3. Journal of Organic Chemistry. 2011, Nov; 76(21): 8944-8954.
  1. 4.   Olefin metathesis in the design and synthesis of a globally constrained Grb2 SH2 domain inhibitor
  2. Gao, Y.; Wei, C. Q.; Burke, T. R.
  3. Organic Letters. 2001 3(11): 1617-1620.
  1. 5.   Designed Epothilones - Combinatorial Synthesis, Tubulin Assembly Properties, and Cytotoxic Action Against Taxol-Resistant Tumor Cells
  2. Nicolaou, K. C.; Vourloumis, D.; Li, T. H.; Pastor, J.; Winssinger, N.; He, Y.; Ninkovic, S.; Sarabia, F.; Vallberg, H.; Roschangar, F.; King, N. P.; Finlay, M. R. V.; Giannakakou, P.; Verdierpinard, P.; Hamel, E.
  3. Angewandte Chemie-International Edition. 1997 36(19): 2097-2103.
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