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PAPERS PUBLISHED IN 1998

This list is arranged by the name of the first author. Any omissions, mistakes and inconsistencies please communicate to the authors of compilation (michal@5z.com). (If you are pointing to any reference, please use its ID# -- the last number in the reference.) You are welcome to use this compilation in your work. Proper way to quote it in your paper is: Lebl M., Leblova Z.: Dynamic database of references in molecular diversity. Internet http://www.5z.com.


Recently added entries are marked in bold

  1. Anonymous. (1998) Combinatorial chemistry promises better catalysts and materials. Chemical Engineering Progress, 94, 11. #11816

  2. Anonymous. (1998) Combinatorial chemistry. Chemical Engineering, 105, 31. #11817

  3. Anonymous. (1998) Simplified characterization of combinatorial libraries. Drug Disc. Today, 3, 483-484. #11815

  4. Abedi, M.R., Caponigro, G., & Kamb, A. (1998) Green fluorescent protein as a scaffold for intracellular presentation of peptides. Nucl. Acid. Res., 26, 623-630. #10582

  5. Ajay, A., Walters, W.P., & Murcko, M.A. (1998) Can we learn to distinguish between "drug-like" and "nondrug-like" molecules? J. Med. Chem., 41, 3314-3324. #11189

  6. Akerblom, E.B., Nygren, A.S., & Agback, K.H. (1998) Six new photolabile linkers for solid-phase synthesis. 1. Methods of preparation. Mol. Diversity, 3, 137-148. #10881

  7. Akporiaye, D.E., Dahl, I.M., Karlsson, A., & Wendelbo, R. (1998) Combinatorial approach to the hydrothermal synthesis of zeolites. Angew. Chem. Int. Ed., 37, 609-611. #11044

  8. Al-Obeidi, F., & Ostrem, J.A. (1998) Factor Xa inhibitors by classical and combinatorial chemistry. Drug Disc. Today, 3, 223-231. #267

  9. Al-Obeidi, F.A., Wu, J.J., & Lam, K.S. (1998) Protein tyrosine kinases: Structure, substrate specificity, and drug discovery. Biopolymers, 47, 197-223. #12299

  10. Albert, R., Knecht, H., Andersen, E., Hungerford, V., Schreier, M.H., & Papageorgiou, C. (1998) Isoxazolylthioamides as potential immunosuppressants a combinatorial chemistry approach. Bioorg. Med. Chem. Lett., 8, 2203-2208. #11187

  11. Alewood, P. (1998) Conotoxins as molecular templates for drug design. In R. Ramage & R. Epton (Eds.), Peptides 1996: Proceedings of the Twenty-Fourth European Peptide Symposium. (pp. 183-186). Mayflower Scientific Ltd., Kingswinford. #11500

  12. Amzel, L.M. (1998) Structure-based drug design. Curr. Opin. Biotechnol., 9, 366-369. #11249

  13. An, H., Haly, B.D., & Cook, P.D. (1998) New piperazinyl polyazacyclophane scaffolds, libraries and biological activities. Bioorg. Med. Chem. Lett., 8, 2345-2350. #11205

  14. An, H., & Cook, P.D. (1998) A solution-phase combinatorial chemistry methodology for drug discovery. Recent Research Developments in Organic Chemistry, 2, 473-488. #13431

  15. An, H.Y., & Cook, P.D. (1998) A solution-phase combinatorial chemistry methodology for drug discovery. Recent Research Developments in Organic Chemistry, 2, 488. #12924

  16. An, H.Y., Wang, T., Mohan, V., Griffey, R.H., & Cook, P.D. (1998) Solution phase combinatorial chemistry. Discovery of 13- and 15-membered polyazapyridinocyclophane libraries with antibacterial activity. Tetrahedron, 54, 3999-4012. #10632

  17. An, H.Y., Haly, B.D., & Cook, P.D. (1998) Discovery of novel pyridinopolyamines with potent antimicrobial activity: Deconvolution of mixtures synthesized by solution-phase combinatorial chemistry. J. Med. Chem., 41, 706-716. #10590

  18. Anderson, E.M., Karin, M., & Kirk, O. (1998) One biocatalyst - many applications: The use of Candida antarctica B-lipase in organic synthesis. Biocatalysis and Biotransformation, 16, 181-204. #12302

  19. Andersson, P.M., Sjostrom, M., & Lundstedt, T. (1998) Preprocessing peptide sequences for multivariate sequence-property analysis. Chemometr. Intell. Lab. Syst., 42, 50. #11818

  20. Andres, C.J., Swann, R.T., Severino, J., Grant-Young, K., Edinger, K., Mongillo, J., & Deshpande, M.S. (1998) A novel parallel distributor for dispensing of Irori(TM) Rf-encoded tags to microkans in 96-well format. Biotech. Bioeng. (Comb. Chem. ), 61, 93-94. #11250

  21. Andres, C.J., Whitehouse, D.L., & Deshpande, M.S. (1998) Transition-metal-mediated reactions in combinatorial synthesis. Curr. Opin. Chem. Biol., 2, 353-362. #12073

  22. Annis, D.A., Helluin, O., & Jacobsen, E.N. (1998) Stereochemistry as a diversity element: Solid-phase synthesis of cyclic RGD peptide derivatives by asymmetric catalysis. Angew. Chem. Int. Ed., 37, 1907-1909. #11251

  23. Apletalina, E., Appel, J., Lamango, N.S., Houghten, R.A., & Lindberg, I. (1998) Identification of inhibitors of prohormone convertases 1 and 2 using a peptide combinatorial library. Journal of Biological Chemistry, 273, 26589-26595. #11819

  24. Appel, J.R., Campbell, G.D., Buencamino, J., Houghten, R.A., & Pinilla, C. (1998) Characterization of antigen-antibody interactions using single substitution analogs and mixture-based synthetic combinatorial libraries. J. Pept. Res., 52, 346-355. #12303

  25. Appell, K.C., Chung, T.D.Y., Solly, K.J., & Chelsky, D. (1998) Biological characterization of neurokinin antagonists discovered through screening of a combinatorial library. J. Biomol. Screen., 3, 19-27. #11158

  26. Arap, W., Pasqualini, R., & Ruoslahti, E. (1998) Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model. Science, 279, 377-380. #10643

  27. Arsequell, G., Espuna, G., Valencia, G., Barluenga, J., Perez Carlon, R., & Gonzalez, J.M. (1998) First aromatic electrophilic iodination reaction on the solid-phase: Iodination of bioactive peptides. Tetrahedron Lett., 39, 7393-7396. #11574

  28. Arza, B., & Felez, J. (1998) The emerging impact of phage display technology in thrombosis and haemostasis [Review]. Thromb. Haemost., 80, 354-365. #11820

  29. Aubagnac, J.L., Enjalbal, C., Subra, G., Bray, A.M., Combarieu, R., & Martinez, J. (1998) Application of time-of-flight secondary ion mass spectrometry to in situ monitoring of solid-phase peptide synthesis on the Multipin(TM) system. J. Mass Spectrom., 33, 1094-1103. #12136

  30. Aubagnac, J.L., Drouot, C., Enjalbal, C., Fulcrand, P., & Martinez, J. (1998) Monitoring of peptides libraries by Fast Atom Bombardment and Electrospray Ionization mass spectrometry. An. Quim., 94, 262-267. #12929

  31. Audet, J., Zandstra, P.W., Eaves, C.J., & Piret, J.M. (1998) Advances in hematopoietic stem cell culture. Curr. Opin. Biotechnol., 9, 146-151. #11111

  32. Ault-Justus, S.E., Hodges, J.C., & Wilson, M.W. (1998) Generation of a library of 4-thiazolidinones utilizing polymer supported quench (PSQ) reagent methodology. Biotech. Bioeng. (Comb. Chem. ), 61, 17-22. #11128

  33. Avdagic, A., & Sunjic, V. (1998) Biocatalytic deracemization of 1,4-benzodiazepines in the synthesis of enantiomerically pure serine. Helv. Chim. Acta, 81, 85-92. #10684

  34. Bailey, D.S., Bondar, A., & Furness, L.M. (1998) Pharmacogenomics: It's not just pharmacogenetics. Curr. Opin. Biotechnol., 9, 595-601. #12304

  35. Baldwin, J.J. (1998) Small molecule libraries: Overview of issues and strategies in library design. In E.M. Gordon & J.F.J. Kerwin (Eds.), Combinatorial Chemistry and Molecular Diversity in Drug Discovery. (pp. 181-188). John Wiley & Sons, New York. #11711

  36. Ball, C.P., Barrett, A.G.M., Commercon, A., Compere, D., Kuhn, C., Roberts, R.S., Smith, M.L., & Venier, O. (1998) Chameleon catches in combinatorial chemistry: Tebbe olefination of polymer supported esters and the synthesis of amines, cyclohexanones, enones, methyl ketones and thiazoles. Chem. Commun., 2019-2020. #11821

  37. Banerjee, A., Lee, K., Yu, Q., Fang, A.G., & Falvey, D.E. (1998) Protecting group release through photoinduced electron transfer: Wavelength control through sensitized irradiation. Tetrahedron Lett., 39, 4635-4638. #10916

  38. Barbaste, M., Rolland-Fulcrand, V., Roumestant, M.L., Viallefont, P., & Martinez, J. (1998) Rapid solid phase synthesis of alpha-amino acids. Tetrahedron Lett., 39, 6287-6290. #11026

  39. Barco, A., Benetti, S., De Risi, C., Marchetti, P., Pollini, G.P., & Zanirato, V. (1998) Polymer-bound 4-benzyl-sulfonyl-1-triphenylphosphoranylidene-2-butanone as a tool for the solid-phase synthesis of substituted piperidin-4-one derivatives. Tetrahedron Lett., 39, 7591-7594. #11565

  40. Barrett, A.G.M., Smith, M.L., & Zecri, F.J. (1998) Impurity annihilation: A strategy for solution phase combinatorial chemistry with minimal purification. Chem. Commun., 2317-2318. #12138

  41. Bartoli, F., Nuzzo, M., Urbanelli, L., Bellintani, F., Prezzi, C., Cortese, R., & Monaci, P. (1998) DNA-based selection and screening of peptide ligands. Nat. Biotech., 16, 1068-1073. #12306

  42. Baudelle, R., Melnyk, P., Deprez, B., & Tartar, A. (1998) Parallel synthesis of polysubstituted tetrahydroquinolines. Tetrahedron, 54, 4125-4140. #10641

  43. Baumbach, W.R., Carrick, T.A., Pausch, M.H., Bingham, B., Carmignac, D., Robinson, I.C.A.F., Houghten, R., Eppler, C.M., Price, L.A., & Zysk, J.R. (1998) A linear hexapeptide somatostatin antagonist blocks somatostatin activity in vitro and influences growth hormone release in rats. Mol. Pharmacol., 54, 864-873. #12307

  44. Bauser, M., Winter, M., Valenti, C.A., Wiesmuller, K.H., & Jung, G. (1998) Synthesis of hydantoins via N,N'-ureas derived from polymer-bound amino acids. Mol. Diversity, 3, 257-260. #12101

  45. Baxter, E.W., Rueter, J.K., Nortey, S.O., & Reitz, A.B. (1998) Arylsulfonate esters in solid phase organic synthesis. II.Compatibility with commonly-used reaction conditions. Tetrahedron Lett., 39, 979-982. #10491

  46. Bayle, D., Wangler, S., Weitzenegger, T., Steinhilber, W., Volz, J., Przybylski, M., Schafer, K.P., Sachs, G., & Melchers, K. (1998) Properties of the P-type ATPases encoded by the copAP operons of Helicobacter pyroli and Helicobacter felis. J. Bacteriol., 180, 317-329. #10812

  47. Behrens, C., & Nielsen, P.E. (1998) A combinatorial approach to new DNA minor groove bonders. Comb. Chem. High Throughput Screening, 1, 127-134. #11758

  48. Bender, L.H. (1998) The oral delivery of macromolecules: 75 Years of need. Innovations in Pharmaceutical Technology, 1, 30-33. #12126

  49. Benedetti, F., Berti, F., Flego, M., Resmini, M., & Bastiani, E. (1998) A competitive immunoassay for the detection of esterolytic activity of antibodies and enzymes. Anal. Biochem., 256, 67-73. #10722

  50. Benson, D.E., Wisz, M.S., & Hellinga, H.W. (1998) The development of new biotechnologies using metalloprotein design. Curr. Opin. Biotechnol., 9, 370-376. #11253

  51. Berg, T., Vandersteen, A.M., & Janda, K.D. (1998) High-throughput synthesis and direct screening for the discovery of novel hydrolytic metal complexes. Bioorg. Med. Chem. Lett., 8, 1221-1224. #10832

  52. Bergbreiter, D.E., Liu, Y.S., Furyk, S., & Case, B.L. (1998) Pd-Catalyzed synthesis of a tethered soluble polymeric phosphine ligand. Tetrahedron Lett., 39, 8799-8802. #11969

  53. Berglund, J., Lindbladh, C., Nicholls, I.A., & Mosbach, K. (1998) Selection of phage display combinatorial library peptides with affinity for a yohimbine imprinted methacrylate polymer. Anal. Commun., 35, 3-7. #10689

  54. Berlin, K., Jain, R.K., & Richert, C. (1998) Are porphyrin mixtures favorable photodynamic anticancer drugs? A model study with combinatorial libraries of tetraphenylporphyrins. Biotech. Bioeng. (Comb. Chem. ), 61, 107-118. #11254

  55. Berlin, K., Jain, R.K., Tetzlaff, C., Steinbeck, C., & Richert, C. (1998) Spectrometrically monitored selection experiments: Quantitative laser desorption mass spectrometry of small chemical libraries [erratum]. Chem. Biol., 4, 237-238. #9957

  56. Berman, J. & Howard, R.J. (1998) Combinatorial drug discovery: Concepts. In E.M. Gordon & J.F.J. Kerwin (Eds.), Combinatorial Chemistry and Molecular Diversity in Drug Discovery. (pp. 447-452). John Wiley & Sons, New York. #11729

  57. Berteina, S., & De Mesmaeker, A. (1998) Application of radical chemistry to solid support synthesis. Tetrahedron Lett., 39, 5759-5762. #10965

  58. Bertini, V., Lucchesini, F., Pocci, M., & De Munno, A. (1998) 1,3-Dithiane polymers for the supported synthesis of ketones. Tetrahedron Lett., 39, 9263-9266. #12019

  59. Beutel, B.A. (1998) Strategies for screening combinatorial libraries. In E.M. Gordon & J.F.J. Kerwin (Eds.), Combinatorial Chemistry and Molecular Diversity in Drug Discovery. (pp. 421-432). John Wiley & Sons, New York. #11727

  60. Bevilacqua, J.M., & Bevilacqua, P.C. (1998) Thermodynamic analysis of an RNA combinatorial library contained in a short hairpin. Biochemistry, 37, 15877-15884. #12311

  61. Bhalay, G., & Dunstan, A.R. (1998) Facile solid phase synthesis of an activated diazo linker. Tetrahedron Lett., 39, 7803-7806. #11577

  62. Bhalay, G., Cowell, D., Hone, N.D., Scobie, M., & Baxter, A.D. (1998) Multiple solid-phase synthesis of hydantoins and thiohydantoins. Mol. Diversity, 3, 195-198. #11255

  63. Bhandari, A., Jones, D.G., Schullek, J.R., Vo, K., Schunk, C.A., Tamanaha, L.L., Chen, D., Yuan, Z., Needels, M.C., & Gallop, M.A. (1998) Exploring structure-activity relationship around the phosphomannose isomerase inhibitor AF14049 via combinatorial synthesis. Bioorg. Med. Chem. Lett., 8, 2303-2308. #11198

  64. Bhat, L., Liu, Y.B., Victory, S.F., Himes, R.H., & Georg, G.I. (1998) Synthesis and evaluation of paclitaxel C7 derivatives: Solution phase synthesis of combinatorial libraries. Bioorg. Med. Chem. Lett., 8, 3181-3186. #12312

  65. Bianco, A., Brock, C., Zabel, C., Walk, T., Walden, P., & Jung, G. (1998) New synthetic non-peptide ligands for classical major histocompatibility complex class I molecules. Journal of Biological Chemistry, 273, 28759-28765. #12314

  66. Bicknell, A.J., Hird, N.W., & Readshaw, S.A. (1998) Efficient robotic synthesis. Multi-component preparation of a tricyclic template by solid phase Tsuge reaction. Tetrahedron Lett., 39, 5869-5872. #10968

  67. Bienayme, H., & Bouzid, K. (1998) Synthesis of rigid hydrophobic tetrazoles using an Ugi multi-component heterocyclic condensation. Tetrahedron Lett., 39, 2735-2738. #10748

  68. Bienayme, H. (1998) "Reagent explosion": An efficient method to increase library size and diversity. Tetrahedron Lett., 39, 4255-4258. #10858

  69. Bienayme, H., & Bouzid, K. (1998) A new heterocyclic multicomponent reaction for the combinatorial synthesis of fused 3-aminoimidazoles. Angew. Chem. Int. Ed., 37, 2234-2237. #11823

  70. Bilodeau, M.T., & Cunningham, A.M. (1998) Solid-supported synthesis of imidazoles: A strategy for direct resin-attachment to the imidazole core. J. Org. Chem., 63, 2800-2801. #10754

  71. Bing, Y. (1998) Monitoring the progress and the yield of solid-phase organic reactions directly on resin supports. Account. Chem. Res., 31, 621-630. #12219

  72. Blackburn, C. (1998) A three-component solid-phase synthesis of 3-aminoimidazol[1,2-a]azines. Tetrahedron Lett., 39, 5469-5472. #10954

  73. Blackburn, C., Guan, B., Fleming, P., Shiosaki, K., & Tsai, S. (1998) Parallel synthesis of 3-aminoimidazol[1,2-a]pyridines and pyrazines by a new three-component condensation. Tetrahedron Lett., 39, 3635-3638. #10845

  74. Blaskovich, M.A., & Kahn, M. (1998) Solid-phase preparation of dienes. J. Org. Chem., 63, 1119-1125. #11798

  75. Blaskovich, M.A., & Kahn, M. (1998) Polymer-supported acetylide addition to hexa-2,4-dienal. Synthesis-Stuttgart, 965-966. #12236

  76. Bleczinski, C.F., & Richert, C. (1998) Monitoring the hybridization of the components of oligonucleotide mixtures to immobilized DNA via matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Rapid Commun. Mass Spectrom., 12, 1737-1743. #12315

  77. Bleicher, K., Lin, M.F., Shapiro, M.J., & Wareing, J.R. (1998) Diffusion edited NMR: Screening compound mixtures by affinity NMR to detect binding ligands to vancomycin. J. Org. Chem., 63, 8486-8490. #12316

  78. Blettner, C.G., Konig, W.A., Stenzel, W., & Schotten, T. (1998) Poly(ethylene glycol) supported liquid phase synthesis of biaryls. Synlett, 295-297. #12125

  79. Blondelle, S.E., Nefzi, A., Ostresh, J.M., & Houghten, R.A. (1998) Novel antifungal compounds derived from heterocyclic positional scanning. Combinatorial libraries. Pure Appl. Chem., 70, 2107-2145. #12907

  80. Boder, E.T., & Wittrup, K.D. (1998) Optimal screening of surface-displayed polypeptide libraries. Biotechnol. Progr., 14, 55-62. #12203

  81. Boeijen, A., & Liskamp, R.M.J. (1998) Sequencing of peptoid peptidomimetics by Edman degradation. Tetrahedron Lett., 39, 3589-3592. #10810

  82. Boeijen, A., Kruijtzer, J.A.W., & Liskamp, R.M.J. (1998) Combinatorial chemistry of hydantoins. Bioorg. Med. Chem. Lett., 8, 2375-2380. #11210

  83. Boesteanu, A., Brehm, M., Mylin, L.M., Christianson, G.J., Tevethia, S.S., Roopenian, D.C., & Joyce, S. (1998) A molecular basis for how a single TCR interfaces multiple ligands. Journal of Immunology, 161, 4719-4727. #12317

  84. Boger, D.L. (1998) Combinatorial chemistry. Bioorg. Med. Chem. Lett., 8, VII-VII. #11824

  85. Boger, D.L., Goldberg, J., Jiang, W.Q., Chai, W.Y., Ducray, P., Lee, J.K., Ozer, R.S., & Andersson, C.M. (1998) Higher order iminodiacetic acid libraries for probing protein-protein interactions. Bioorg. Med. Chem., 6, 1347-1378. #11825

  86. Boger, D.L., Ducray, P., Chai, W., Jiang, W., & Goldberg, J. (1998) Higher order iminodiacetic acid libraries for probing protein-protein interactions. Bioorg. Med. Chem. Lett., 8, 2339-2344. #11204

  87. Boger, D.L., Chai, W., & Jin, Q. (1998) Multistep convergent solution-phase combinatorial synthesis and deletion synthesis deconvolution. J. Amer. Chem. Soc., 120, 7220-7225. #11014

  88. Boger, D.L., & Chai, W. (1998) Solution-phase combinatorial synthesis: Convergent multiplication of diversity via the olefin metathesis reaction. Tetrahedron, 54, 3955-3970. #10629

  89. Bohm, H.J. (1998) Combinatorial docking. In H. van de Waterbeemd, B. Testa & G. Folkers (Eds.), Computer-Assisted Lead Finding and Optimization. (pp. 123-133). Verlag Helvetica Chimica Acta and VCH, Basel and Weinheim. #11379

  90. Bolli, M.H., & Ley, S.V. (1998) Development of a polymer bound Wittig reaction and use in multi-step organic synthesis for the overall conversion of alcohols to b-hydroxyamines. J. Chem. Soc. Perkin Trans. 1, 1, 2243-2246. #13438

  91. Bols, M. (1998) 1-Aza sugars, apparent transition state analogues of equatorial glycoside formation/cleavage [review]. Account. Chem. Res., 31, 1-8. #10685

  92. Bondy, S.S. (1998) The role of automation in drug discovery. Curr. Opin. Drug. Disc. Develop., 1, 116-119. #11395

  93. Borman, S. (1998) Beetles do it combinatorially. Bugs combine simple precursors to make library of novel defensive compounds. C&EN, 76, 11-11. #10876

  94. Borman, S. (1998) Combinatorial carbohydrates. Prospects are looking sweet for use of sugar-based combinatorial libraries to find novel bioactive substances. C&EN, 76, 49-52. #10877

  95. Borman, S. (1998) Biosynthesis, combinatorially. A variety of techniques nudge microbes to produce 'unnatural' natural products. C&EN, 76, 29-30. #11583

  96. Boudjennah, L., Daletfumeron, V., & Pagano, M. (1998) Expression of collagenase/gelatinase activity from basement-membrane fibronectin: Isolation after limited proteolysis of a bovine lens capsule and molecular definition of this thiol-dependent zinc metalloproteinase. Eur. J. Biochem., 255, 246-254. #11256

  97. Boussie, T.R., Coutard, C., Turner, H., Murphy, V., & Powers, T.S. (1998) Solid-phase synthesis and encoding strategies for olefin polymerization catalyst libraries. Angew. Chem. Int. Ed., 37, 3272-3275. #12139

  98. Boyd, D.B. (1998) Innovation and the rational design of drugs. Chemtech, 28, 19-23. #11584

  99. Boyd, D.B. (1998) Rational drug design: Controlling the size of the haystack. Mod. Drug Dis., 1, 41-48. #12277

  100. Brandli, C., & Ward, T.R. (1998) Libraries via metathesis of internal olefins. Helv. Chim. Acta, 81, 1616-1621. #13439

  101. Bray, A.M., Maeji, N.J., Lagniton, L.M., Chiefari, D., James, I.W., Ang, K., Ede, N., Valerio, R.M. & Mason, T.J. (1998) Simultaneous multiple synthesis by the Multipin(TM) method: Techniques for multiple handling,high throughput characterization and reaction optimization on solid phase. In X. Xu, Y. Ye & J.P. Tam (Eds.), Peptides. Biology and Chemistry. Proceedings of the 1996 Chinese Peptide Symposium. (pp. 67. Kluwer/ESCOM, Dordrecht. #14303

  102. Breitenbucher, J.G., Johnson, C.R., Haight, M., & Phelan, J.C. (1998) Generation of a piperazine-2-carboxamide library: A practical application of the phenol-sulfide react and release linker. Tetrahedron Lett., 39, 1295-1298. #10510

  103. Breitenbucher, J.G., & Hui, H.C. (1998) Titanium mediated reductive amination on solid support: Extending the utility of the 4-hydroxy-thiophenol linker. Tetrahedron Lett., 39, 8207-8210. #12009

  104. Brennan, T., Biddison, G., Frauendorf, A., Schwarcz, L., Keen, B., Ecker, D.J., Davis, P.W., Tinder, R., & Swayze, E.E. (1998) Two-dimensional parallel array technology as a new approach to automated combinatorial solid-phase organic synthesis. Biotech. Bioeng. (Comb. Chem. ), 61, 33-45. #10759

  105. Bridonneau, P., Chang, Y.F., O'Connell, D., Gill, S.C., Snyder, D.W., Johnson, L., Goodson, T.Jr., Herron, D.K., & Parma, D.H. (1998) High-affinity aptamers selectively inhibit human nonpancreatic secretory phospholipase A2 (hnps-PLA2). J. Med. Chem., 41, 778-786. #11173

  106. Brill, W.K.D., De Mesmaeker, A., & Wendeborn, S. (1998) Solid phase synthesis of levoglucosan derivatives. Synlett, 1085-1090. #12318

  107. Brill, W.K.D., Schmidt, E., & Tommasi, R.A. (1998) Immobilizations of nucleophiles on polystyrene supports. Synlett, 906. #11258

  108. Brocchini, S., James, K., Tangpasuthadol, V., & Kohn, J. (1998) Structure-property correlations in a combinatorial library of degradable biomaterials. J. Biomed. Material. Res., 42, 66-75. #11827

  109. Broderick, S., Davis, A.P., & Williams, R.P. (1998) The "triamino-analogue" of methyl cholate: A facial amphiphile and scaffold with potential for combinatorial and molecular recognition chemistry. Tetrahedron Lett., 39, 6083-6086. #10992

  110. Bromidge, S., Wilson, P.C., & Whiting, A. (1998) A parallel combinatorial approach to locating homochiral Lewis acid catalysts for the asymmetric aza-Diels-Alder reaction of an imino dienophile. Tetrahedron Lett., 39, 8905-8908. #11970

  111. Brown, A.R., Hermkens, P.H.H., Ottenheijm, H.C.J., & Rees, D.C. (1998) Solid phase synthesis. Synlett, 817-827. #11260

  112. Brown, D.S., Revill, J.M., & Shute, R.E. (1998) Merrifield, alpha-methoxyphenyl (MAMP) resin: A new versatile solid support for the synthesis of secondary amides. Tetrahedron Lett., 39, 8533-8536. #11946

  113. Brown, R.C.D. (1998) Recent developments in solid-phase organic synthesis. J. Chem. Soc. Perkin Trans. 1, 3293-3320. #11829

  114. Brown, R.D., & Clark, D.E. (1998) Genetic diversity: applications of evolutionary algorithms to combinatorial library design. Exp. Opin. Ther. Patents, 8, 1447-1459. #12320

  115. Buchholz, C.J., Peng, K.W., Morling, F.J., Zhang, J., Cosset, F.L., & Russell, S.J. (1998) In vivo selection of protease cleavage sites from retrovirus display libraries. Nat. Biotech., 16, 951-954. #11830

  116. Buckman, B.O., Morrissey, M.M., & Mohan, R. (1998) Solution-phase parallel synthesis of benzoxazines using a polymer-supported carbodiimide. Tetrahedron Lett., 39, 1487-1488. #10518

  117. Bunin, B.A. (1998) The Combinatorial Index. Academic Press, San Diego. ISBN 0121413403 #10496

  118. Bures, M.G., & Martin, Y.C. (1998) Computational methods in molecular diversity and combinatorial chemistry. Curr. Opin. Chem. Biol., 2, 376-380. #12076

  119. Burioni, R., Plaisant, P., Bugli, F., Solforosi, L., Carri, V.D., Varaldo, P.E., & Fadda, G. (1998) A new subtraction technique for molecular cloning of rare antiviral antibody specificities from phage display libraries. Res. Virol., 149, 327-330. #12322

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