Wayne K. Anderson

• El-Araby, M. E.; Bernacki, R. J.; Makara, G. M.; Pera, P. J.; Anderson, W. K. Biorg. Med. Chem., 2004, 12 (11), 2867-2879. Synthesis, Molecular Modeling and Evaluation of Non-Phenolic Indole Analogs of Mycophenolic Acid.
  
• Campbell, W. H.; Anderson, W. K.; Burckart, G. J.; Clark, A. M.; DiGate, R. J.; Lee, V. H. L.; Rogers, M. E.; Miller, K. W. Am. J. Pharm. Ed., 2002, 66, 28S-33S. Institutional and faculty roles and responsibilities in the emerging environment of university-wide interdisciplinary research structures: Report of the 2001-2002 Research and Graduate Affairs Committee.
  
• Bhamare, N. K.; Lai, G.; Anderson, W. K. J. Chem Res. (S), 2002, 110-111. Ene-type chlorination of functionalized olefins using sulfuryl chloride in the absence of base.
  
• Lai, G. F.; Bhamare, N. K.; Anderson, W. K. SYNLETT 2001 (2): 230-231. A one-pot method for the efficient preparation of aromatic nitriles from aldehydes using ammonia, magnesium sulfate, and manganese dioxide.
  
• Anderson, W. K.; Wahler, R. G. Aging Today, 2001, 22(1), 3-8. Pharmacy Management can Reduce Medicare and Human Costs.
  Lai, G. and Anderson, W. K. Tetrahedron, 2000, 2583-2590. Synthesis of Novel Analogues of Mycophenolic Acid as Potential Antineoplastic Agents.
  
• Lai, G. F.; Anderson, W. K. Syn. Commun. 1997, 27 (7): 1281-1283. A simplified procedure for the efficient conversion of aromatic aldehydes into esters.
  
• Makara, G. M.; Klubek, K.; Anderson, W. K. Syn. Commun. 1996, 26, 1935-1942. An Improved Synthesis of 5,7-dimethoxy-4-methylphthalide, a Key Intermediate in the Synthesis of Mycophenolic Acid.
  
• Makara, G. M.; Keseru, G. M.; Kajtár-Peredy, M.; Anderson, W. K. J. Med. Chem. 1996, 39, 1236-1242 Nuclear Magnetic Resonance and Molecular Modeling Study on Mycophenolic Acid: Implications for Binding to Inosine Monophosphate Dehydrogenase.
  
• Makara, G. M.; Klubek, K.; Anderson, W. K. Syn. Commun. 1996, 26, 1935-1942. An Improved Synthesis of 5,7-dimethoxy-4-methylphthalide, a Key Intermediate in the Synthesis of Mycophenolic Acid.
• Makara, G. M.; Keseru, G. M.; Kajtar-Peredy, M.; Anderson, W. K. J. Med. Chem.1996, 39, 1236-1242. NMR and Molecular Modeling Study on Mycophenolic Acid: Implications for Binding to Inosine Monophosphate Dehydrogenase.
  
• Anderson, W. K.; Boehm, T. L.; Makara, G.; Swann, R. T. J. Med. Chem. 1996, 39, 46-55. Synthesis and Modeling Studies with Monocyclic Analogues of Mycophenolic Acid.
  
• Anderson, W. K.; Kasliwal, R.; Houston, D. M.; Wang, Y. -S.; Narayanan, V. L.; Haugwitz, R. D.; Plowman, J. J. Med. Chem. 1995, 38, 3789-3797. Synthesis, Antitumor Activity and Chemical Properties of Silaplatin and Related Platinum(II) and Platinum(IV) Complexes Derived from beta-Silylamines.
  
• Lai, G. F.; Anderson, W. K. Syn. Commun. 1995, 25 4086-4091. Facile Preparation of Substituted Allenic Esters via the Ortho Ester Claisen Rearrangement.
• Anderson, W. K.; Lai, G. Synthesis 1995, 1287-1290. Boron Trifluoride-Diethyl Ether Complex Catalyzed Aromatic Amino-Claisen Rearrangements.
  
• Makara, G. M.; Anderson, W. K. J. Org. Chem., 1995, 60, 5717-5718. An efficient synthesis of 5,7-dimethoxy-4-methylphthalide, a key intermediate in the synthesis of mycophenolic acid.
• Lee, J.; Anderson, W. K. Biorg. Med. Chem. Lett. 1995, 5, 861-866. Design and Synthesis of Heterocyclic Analogues of Mycophenolic Acid as Potential Chemotherapeutic Agents.
  
• Anderson, W. K.; Tan, P. Syn. Commun. 1994, 24, 3081-3089. Oxidative Degradation of Castanospermine.
  
• Anderson, W. K.; Gopalsamy, A.; Reddy, P. S. J. Med. Chem. 1994, 37, 1955-1963. Design, Synthesis and Study of 9-Substituted Ellipticine and 2-Methylellipticinium Analogues as Potential CNS-Selective Antitumor Agents.
  
• Anderson, W. K.; Dalvie, D. K. J. Heterocycl. Chem. 1993, 30, 1533-1536. Synthesis of 4-(2-Chloroethyl)-2,3-dihydro[1,4]oxazino[2,3-b]quinoline and 4-(2-Chloroethyl)-2,3-dihydropyrido[2,3-b]-[1,4]oxazine.
  
• Anderson, W. K.; Houston, D. M.; Jarosinski, M. A.; Kinder, F. K., Jr.; Kode, R. N.; Van Roey, P.; Salerno, J. M. Drug Dev. Res. 1993, 30, 143-146. Structure, Synthesis, and Antitumor Activity of the Hydrolysis Product of the Antitumor Agent Carmethizole.
  
• Lai, G.; Anderson, W. K. Tetrahedron Lett. 1993, 34, 6849-6852. A Concise Synthesis of a Benzimidazole Analogue of Mycophenolic Acid using a BF₃.Et₂O Catalyzed Amino-Claisen Rearrangement.
  
• Jarosinski, M. A.; Reddy, P. S. Anderson, W. K. J. Med. Chem. 1993, 36, 3618-3627. Synthesis, Chemical Reactivity, and Antitumor Evaluation of Congeners of Carmethizole Hydrochloride, an Experimental Acylated Vinylogous Carbinolamine Tumor Inhibitor.
  
• Anderson, W. K.; Gopalsamy, A.; Reddy, P. S. Proc. 3rd Korea-Japan Joint Symposium on Drug Design and Development. 1993, 73-78. The Development of New Anticancer Drugs from Lead Structures.
  
• Waud, W. R.; Plowman, J,; Garrison, S. D. Jr.; Dykes, D. J.; Anderson, W. K.; Griswold, D. P. Jr. Cancer Chemother. Pharmacol. 1992, 30, 261-266. Antitumor Activity and Cross-Resistance of Carmethizole Hydrochloride (NSC 602668) in Preclinical Models in Mice.
  
• Lee, J.; Anderson, W. K. Syn. Commun. 1992, 22, 369-376. A Facile Synthesis of an (E)-4-Methyl-4-hexenoic Acid Substituted Pyridine Analogue of Mycophenolic Acid.
  
• Anderson, W. K.; Lee, J.; Swann, R. T.; Boehm, T. L. in, Advances in New Drug Development; Kim, B.-K.; Lee, E. B.; Kim, C.-K.; Han, Y. N. Eds.; The Pharmaceutical Society of Korea: Seoul, Korea, 1991; pp 8-17. The Design, Synthesis and Study of Mycophenolic acid Analogues as Potential Inhibitors of Inosine Monophosphate Dehydrogenase.
  
• Kinder, F. K.; Jarosinski, M. A.; Anderson, W. K. J. Org. Chem. 1991, 56, 6475-6477. Synthesis of 3-Pyrrolines by an Intramolecular Wittig Reaction.
  
• Elliott, W. L.; Fry, D. W.; Anderson, W. K.; Nelson, J. M.; Hook, K. E.; Hawkins, P. A.; Leopold, W. R. III Cancer Res. 1991, 51, 4581-4587. In vivo and in vitro Evaluation of the Alkylating Agent Carmethizole.
  
• Gopalsamy, A.; Anderson, W. K. Tetrahedron Lett. 1991, 32, 4669-4670. Facile Acyl Migration in 6-O-Acylcastanospermine.
  
• Jarosinski, M. A.; Anderson, W. K. J. Org. Chem. 1991, 56, 4058-4062. Preparation of Noncondensed 2-Substituted 1-Methylimidazoles via Ipso-Substitution Reaction on 2-Sulfinyl or 2-Sulfonyl Derivatives of 4,5-Disubstituted 1-Methylimidazoles.
  
• Stella, V. J.; Anderson, W. K.; Benedetti, A.; Waugh, W. A.; Killion, R. B. Jr. Int. J. Pharm. 1991, 71, 157-165. Stability of Carmethizole Hydrochloride (NSC-602668), an Experimental Cytotoxic Agent.
  
• Haugwitz, R. D.; Anderson, W. K.; Plowman, J.; Kasliwal, R.; Houston, D. M.; Narayanan, V. L. Appl. Organometallic Chem. 1990, 4, 375. [bis(aminomethyl)dimethylsilane] -Pt(II)dichloride: A Potential Antitumor Agent.
  
• Lee, H.; Anderson, W. K. Tetrahedron Lett. 1990, 31, 4405. Total Synthesis of 4-Acetoxymethyl-1,6,9-trimethyl-1,9-diazaanthracene-2,5,8,10-tetraone, a Nybomycin Acetate Analogue.
  
• Anderson, W. K.; Mach, R. H. J. Heterocycl. Chem. 1990, 27, 1025. Synthesis and Chemical Reactivity of C-5 Substituted 6,7-bis(hydroxymethyl)-1H-pyrrolizine Biscarbamate Tumor Inhibitors.
  
• Anderson, W. K.; Kinder, F. K., Jr. J. Heterocycl. Chem. 1990, 27, 975. Synthesis of 3,9b-Dihydro-5H-pyrrolo[2,1-a]isoindoles and 3,5,6,10b-Tetrahydropyrrolo[2,1-a]isoquinolines with 1,3-Dipolar Cycloaddition Reactions.
  
• Anderson, W. K.; Dean, D. C.; Endo, T. J. Med. Chem. 1990, 33, 1667. Synthesis, Chemistry, and Antineoplastic Activity of alpha-Halopyridinium Salts: Potential Pyridone Prodrugs of Acylated Vinylogous Carbinolamine Tumor Inhibitors.
  
• Anderson, W. K.; Coburn, R. A.; Gopalsamy, A.; Howe, T. J. Tetrahedron Lett. 1990, 31, 169. A Facile Selective Acylation of Castanospermine.