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Pure Appl. Chem., Vol. 71, No. 12, pp. 2349-2365, 1999

Glossary of Terms Used in Combinatorial Chemistry


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  1. McKeown, S.C.; Watson, S.P.; Carr, R.A.E.; Marshall, P.: A photolabile carbamate based dual linker analytical construct for facile monitoring of solid phase chemistry: ‘TLC’ for solid phase?; Tetrahedron Lett. 1999, 40, 2407-2410

  2. Geysen, H.M.; Wagner, C.D.; Bodnar, W.M.; Markworth, C.J.; Parke, G.J.; Schoenen, F.J.; Wagner, D.S.; Kinder, D.S.: Isotope or mass encoding of combinatorial libraries; Chem. Biol. 1996, 3, 679-688

  3. Carrasco, M.R.; Fitzgerald, M.C.; Oda, Y.; Kent, B.H.: Direct monitoring of organic reactions on solid supports; Tetrahedron Lett. 1997, 38, 6331-6334

  4. Tuerk, C., Gold, L.: Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase; Science 1990, 249, 505-510

  5. Ellington, A.D., Szostak, J.W.: In vitro selection of RNA molecules that bind specific ligands; Nature 1990, 346, 818-822

  6. Osborne, S.E.; Ellington, A.D.: Nucleic acid selection and the challenge of combinatorial chemistry; Chem. Rev. 1997, 97, 349-370

  7. Gooding, G.W.; Baudart, S.; Deegan, T.L.; Heisler, K.; Labadie, J.W.; Newcomb, W.S.; Porco, J.A. Jr.; van Eikeren, P.: On the development of new poly(styrene-oxyethylene) graft copolymer resin supports for solid-phase organic synthesis; J. Comb. Chem. 1999, 1, 113-122

  8. Geysen, H.M.; Rodda, S.J.; Mason, T.J.: A priori delineation of a peptide which mimics a discontinuous antigenic determinant; Mol. Immunol. 1986, 23, 709-15

  9. DeWitt, S.H.; Kiely, J.S.; Stankovic, C.J.; Schroeder, M.C.; Reynolds-Cody, D.M.; Pavia, M.R.: "Diversomers": an approach to nonpeptide, nonoligomeric chemical diversity; Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 6909-6913

  10. Pirrung, M.C.: Spatially addressable combinatorial libraries; Chem. Rev. 1997, 97, 473-488

  11. Zhao, P.-L.; Zambias, R.; Bolognese, J.A.; Boulton, D.; Chapman, K.: Two new criteria for choosing sample size in combinatorial chemistry; Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 10212-10216

  12. Martin, E.J.; Critchlow, R.E.: Beyond mere diversity: tailoring combinatorial libraries for drug discovery; J. Comb. Chem. 1999, 1, 32-45

  13. Ohlmeyer, M.H.J.; Swanson, R.N.; Dillard, L.W.; Reader, J.C.; Asouline, G.; Kobayashi, R.; Wigler, M.; Still, W.C.: Complex synthetic chemical libraries indexed with molecular tags; Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 10922-10926

  14. Instructions to Authors, J. Comb. Chem. 1999, 1, 11A

  15. Downs, G.M.; Willett, P.; Fisanick, W.: Similarity searching and clustering of chemical structure databases using molecular property data; J. Chem. Inf. Comput. Sci. 1994, 34, 1094-1102

  16. Brown, R.D; Martin, Y.C.: Use of structure-activity data to compare structure-based clustering methods and descriptors for use in compound selection: J. Chem. Inf. Comput. Sci. 1996, 36, 572-584

  17. Gorse, D.; Rees, A.; Kaczorek, M.; Lahana, R.: Molecular diversity and its analysis; Drug Discovery Today 1999, 4, 257-264

  18. Sherrington, D.C.: Preparation, structure, and morphology of polymer supports; Chem. Commun. 1998, 2275-2286

  19. Gordon, D.W.; Steele, J.: Reductive alkylation on a solid phase: Synthesis of a piperazinedione combinatorial library; Biorg. Med. Chem. Lett. 1995, 5, 47-50

  20. Szardenings, A.K.; Burkoth, T.S.; Lu, H.H.; Tien, D.W.; Campbell, D.A.: A simple procedure for the solid phase synthesis of diketopiperazine and diketomorpholine derivatives; Tetrahedron 1997, 53, 6573-6593

  21. Czarnik, A.W.: Encoding methods for combinatorial chemistry; Curr. Opin. Chem. Biol. 1997, 1, 60-66

  22. Houghten, R.A.; Pinella, C.; Blondelle, S.E.; Appel, J.R.; Dooley, C.T.; Cuervo, J.H.: Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery; Nature 1991, 354, 84-86

  23. Konings, D.A.M.; Wyatt, J.R.; Ecker, D.J.; Freier, S.M.: Deconvolution of combinatorial libraries for drug discovery: Theoretical comparison of pooling strategies; J. Med. Chem. 1996, 39, 2710-2719

  24. Wilson-Lingardo, L.; Davis, P.W.; Ecker, D.J.; Hebert, N.; Acevedo, O.; Sprankle, K.; Brennan, T.; Schwarcz, L.; Freier, S.M.; Wyatt, J.R.: Deconvolution of combinatorial libraries for drug discovery: Experimental comparison of pooling strategies; J. Med. Chem. 1996, 39, 2720-2726

  25. Tomalia, D.A.; Baker, H.; Dewald, J.; Hall, M.; Kallos, G.; Martin, S.; Roeck, J.; Ryder, J.; Smith, P.: Dendritic macromolecules: Synthesis of starburst dendrimers; Macromolecules 1986, 19, 2466-2468

  26. Schultz J.L.; Wilks, E.S.: Dendritic and star polymers: Classification, nomenclature, structure representation, and registration in the DuPont SCION database; J. Chem. Inf. Comput. Sci. 1998, 38, 85-99

  27. Kim, R.M.; Manna, M.; Hutchins, S.M.; Griffin, P.R.; Yates, N.A.; Bernick, A.M.; Chapman, K.T.: Dendrimer-supported combinatorial chemistry; Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 10012-10017

  28. Swali, V.; Wells, N.J.; Landley, G.J.; Bradley, M.: Solid-phase dendrimer synthesis and the generation of super-high-loading resin beads for combinatorial chemistry; J. Org. Chem. 1997, 62, 4902-4903

  29. Pickett, S.D.; Luttmann, C.; Guerin, V.; Laoui, A.; James, E.: DIVSEL and COMPLIB - Strategies for the design and comparison of combinatorial libraries using pharmacophoric descriptors; J. Chem. Inf. Comput. Sci. 1998, 38, 144-150

  30. Xue, L.; Godden, J.; Gao, H.; Bajorath, J.: Identification of a preferred set of molecular descriptors for compound classification based on principal components analysis; J. Chem. Inf. Comput. Sci. 1999, 39, 699-704

  31. Szardenings A.K.; Antonenko V.; Campbell D.A.; DeFrancisco N.; Ida S.; Shi L.; Sharkov N.; Tien D.; Wang Y.; Navre M.: Identification of highly selective inhibitors of collagenase-1 from combinatorial libraries of diketopiperazines; J. Med. Chem. 1999, 42, 1348-1357

  32. Patel, D.V.; Campbell, D.A.: Protease inhibitor libraries, in Combinatorial Chemistry and Molecular Diversity in Drug Discovery; Gordon, E.M. and Kerwin, J.F.Jr. eds., Wiley-Liss 1998, 189-199

  33. Spaller, M.R.; Burger, M.T.; Fardis, M.; Bartlett, P.A.: Synthetic strategies in combinatorial chemistry; Curr. Opin. Chem. Biol. 1997, 1, 47-53

  34. Baldwin, J.J.; Horlbeck, E.G.: Synthesis of combinatorial libraries; U.S. Patent 5,663,046

  35. Guiles, J.W.; Lanter, C.L.; Rivero, R.A.:A visual tagging process for mix and sort combinatorial chemistry; Angew. Chem. Int. Ed. 1998, 37, 926-928

  36. Xiao, X.-Y.; Zhao, C.; Potash, H.; Nova, M.P.: Combinatorial chemistry with laser optical encoding; Angew. Chem. Int. Ed. Engl. 1997, 36, 780-781

  37. Martin, Y.C.; Brown, R.D.; Bures, M.G.: "Quantifying diversity", in Combinatorial Chemistry and Molecular Diversity in Drug Discovery; Gordon, E.M. and Kerwin, J.F.Jr. eds., Wiley-Liss 1998, 369-385

  38. Ganesan A.: Strategies for the dynamic integration of combinatorial synthesis and screening; Angew. Chem. Intl. Ed. 1998, 37, 2828-2831

  39. Eliseev, A.V.; Nelen, M.I.: Use of molecular recognition to drive chemical evolution: Mechanisms of an automated genetic algorithm implementation Chem. Eur. J. 1998, 4, 825-834

  40. McGregor, M.J.; Muskal, S.M.: Pharmacophore fingerprinting 1. Application to QSAR and focused library design; J. Chem. Inf. Comput. Sci. 1999, 39, 569-574

  41. Nolan, J.; Laver, S.; Prossnitz, E.R.; Sklar, L.A.: Flow cytometry: A versatile tool for all stages of drug discovery; Drug Discovery Today 1999, 4, 173-180

  42. Hird, N.W.: Automated synthesis: New tools for the organic chemist; Drug Discovery Today 1999, 4, 265-274

  43. Curran, D.P.: Strategy-level separation in organic synthesis: From planning to practice; Angew. Chem. Int. Ed. 1998, 37, 1174-1196

  44. Schriemer, D.C.; Bundle, D.R.; Li, L.; Hindsgaul, O.: Micro-scale frontal affinity chromatography with mass spectrometric detection: A new method for the screening of compound libraries; Angew. Chem. Int. Ed. 1998, 37, 3383-3387

  45. Look, G.C.; Holmes, C.P.; Chinn, J.P.; Gallop, M.A.: Methods for combinatorial organic-synthesis - The use of fast C-13 NMR analysis for gel phase reaction monitoring; J. Org. Chem. 1994, 59, 7588-7590

  46. Ellman, J.A.: Design, synthesis, and evaluation of small-molecule libraries; Acc. Chem. Res. 1996, 29, 132-143

  47. Weber, L.: Applications of genetic algorithms in molecular diversity; Curr. Opin. Chem. Biol. 1998, 2, 381-385

  48. Sheridan, R.P.; Kearsley, S.K.: Using a genetic algorithm to suggest combinatorial libraries; J. Chem. Inf. Comput. Sci. 1995, 35, 310-320

  49. Willett, P.: Genetic algorithms in molecular recognition and design; Trends Biotech. 1995, 13, 516-521

  50. Dove, A.: Drug screening — Beyond the bottleneck; Nature Biotech. 1999, 17, 859-863

  51. Taylor, S.J.; Morken, J.P.: Thermographic selection of effective catalysts from an encoded polymer-bound library; Science 1998, 280, 267-270

  52. Kaiser, E.; Colescott, R.L.; Bossing, C.D.; Cook, P.I. Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides; Anal. Biochem. 1970, 34, 595-598

  53. Sarin, V.K.; Kent, S.B.H.; Tam, J.P.; Merrifield, R.B. Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction; Anal. Biochem. 1981, 117, 147-157

  54. Bernatowicz, M.S.; Daniels, S.B.; Koster, H. A comparison of acid labile linkage agents for the synthesis of peptide C-terminal amides; Tetrahedron Lett. 1989, 30, 4645-4648

  55. St. Hilaire, P.M.; Lowary, T.L.; Meldal, M.; Bock, K.: Oligosaccharide mimetics obtained by novel, rapid screening of carboxylic acid encoded glycopeptide libraries; J. Am. Chem. Soc. 1998, 120, 13312-13320

  56. Ostresh, J.M.; Husar, G.M.; Blondelle, S.E.; Dorner, B.; Weber, P.A.; Houghten, R.A.: "Libraries from libraries": Chemical transformation of combinatorial libraries to extend the range and repertoire of chemical diversity; Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 11138-11142

  57. Backes, B.J.; Ellman, J.A.: Solid support linker strategies; Curr. Opinion. Chem. Biol. 1997, 1, 86-93

  58. Bayer, E.; Mutter, M.: Liquid phase synthesis of peptides; Nature (London) 1972, 237, 512-513

  59. Gravert, D.J.; Janda, K.D.: Organic synthesis on soluble polymer supports: Liquid phase methodologies; Chem. Rev. 1997, 97, 489-510

  60. Keifer, P.A.: Influence of resin structure, tether length, and solvent upon the high-resolution 1H NMR spectra of solid-phase-synthesis resins; J. Org. Chem. 1996, 61, 1558-1559

  61. Fodor, S.P.A.; Leighton, R.J.; Pirrung, M.C.; Stryer, L.; Lu, A.T.; Solas, D.: Light-directed, spatially addressable parallel chemical synthesis; Science 1991, 251, 767-773

  62. Briceno, G.; Chang, H.; Sun, X.; Schultz, P.G.; Xiang, X.D. A class of cobalt oxide magnetoresistance materials discovered with combinatorial synthesis. Science 1995, 270, 273-275

  63. Merrifield, R.B.: Solid-Phase Peptide Synthesis. 1. The synthesis of a tetrapeptide; J. Am. Chem. Soc. 1963, 85, 2149-2154

  64. Gasteiger, J.; Zupan, J.: Neural networks for chemists: An introduction. VCH, Weinheim, 1993

  65. Gasteiger, J.; Zupan, J.: Neural networks in chemistry; Angew. Chem. Int. Ed. Engl. 1993, 32, 503-527

  66. Furka, A.: Sub-library composition of peptide libraries: potential application in screening; Drug Dev. Res. 1994, 33, 90-97

  67. Pirrung, M.C.; Chen J.: Preparation and screening against acetylcholinesterase of a non-peptide "indexed" combinatorial library; J. Am. Chem. Soc. 1995, 117, 1240-1245

  68. Déprez, B.; Williard, X.; Bourel, L.; Coste, H.; Hyafil, F.; Tartar, A.: Orthogonal combinatorial chemical libraries; J. Am. Chem. Soc. 1995, 117, 5405-5406

  69. Erb, E.; Janda, K.D.; Brenner, S.: Recursive deconvolution of combinatorial chemical libraries. Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 11422-11426

  70. Lebl, M.; Pátek, M.; Koi_, P.; KrchHák, V.; Hruby, V.J.; Salmon, S. E.; Lam, K.S., Multiple release of equimolar amounts of peptides from a polymeric carrier using orthogonal linkage-cleavage chemistry. Int. J. Peptide. Prot. Res. 1993, 41, 201-203

  71. Baldwin, J.J.; Burbaum, J.J.; Henderson, I.; Ohlmeyer, M.H.J.: Synthesis of a small molecule combinatorial library encoded with molecular tags; J. Am. Chem. Soc. 1995, 117, 5588-5589

  72. Zuckerman, R.N.; Kerr, J.M.; Kent, S.B.H.; Moos, W.H.: Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by sub-monomer solid-phase synthesis; J. Am. Chem. Soc. 1992, 114, 10646-10647

  73. Zuckermann, R.N.; Martin, E.J.; Spellmeyer, D.C.; Stauber, G.B.; Shoemaker, K.R.; Kerr, J.M.; Figliozzi, G.M.; Goff, D.A.; Siani, M.A.; Simon, R.J.; Banville, S.J.; Brown, E.G.; Wang, L.; Richter, L.S.; Moos, W.H.: Discovery of nanomolar ligands for 7-transmembrane G-protein-coupled receptors from a diverse (N-substituted) glycine peptoid library; J. Med. Chem. 1994, 37, 2678-2685

  74. Cwirla, S.; Peters, E.A.; Barrett, R.W.; Dower, W.J. Peptides on phage: a vast library of peptides for identifying ligands: Proc. Natl. Acad. Sci. U.S.A. 1990, 87, 6378-6382

  75. Scott, J.K.; Smith, G.P.: Searching for peptide ligands with an epitope library; Science 1990, 249, 386-390

  76. Smith, G.P.; Petrenko, V.A.: Phage display; Chem. Rev. 1997, 97, 391-410

  77. Wermuth, C.; Ganellin, C.R.; Lindberg, P.; Mitscher, L.: Glossary of terms used in medicinal chemistry (IUPAC recommendations 1998); Pure. Appl. Chem. 1998, 70, 1129-1143

  78. Wermuth, C.; Langer, T.: Pharmacophore identification. In 3D QSAR in Drug Design; Kubinyi, H. ed.; Escom, Leiden. 1998, 117-136

  79. Furka, A.; Bennett, W.D.: Combinatorial libraries by portioning and mixing; Comb. Chem. High Throughput Screening 1999, 2, 105-122

  80. Lam, K.S.; Lebl, M.; KrchHák, V.: The "one-bead-one-compound" combinatorial library method; Chem. Rev. 1997, 97, 411-448

  81. Pinilla, C.; Appel, J.; Blondelle, S.E.; Dooley, C.T.; Dorner, B.; Eichler, J.; Ostresh, J.M.; Houghten, R.A.: A review of the utility of soluble peptide combinatorial libraries; Biopolymers (Peptide Science) 1995, 37, 221-240

  82. Jonsson, J.; Eriksson, L.; Hellberg, S.; Sjostrom, M.; Wold, S.: Multivariate parametrization of 55 coded and non-coded amino acids; Quant. Struct.-Act. Relat. 1989, 8, 204-209

  83. Evans, B.E.; Rittle, K.E.; Bock, M.G.; DiPardo, R.M.; Freidinger, R.M.; Whitter, W.L.; Lundell, G.F.; Veber, D.F.; Anderson, P.S.; Chang, R.S.: Methods for drug discovery: Development of potent, selective, orally effective cholecystokinin antagonists; J. Med. Chem. 1988, 31, 2235-2246

  84. Nicolaou, K.C.; Xiao, X.-Y.; Parandoosh, Z.; Senyei, A.; Nova, M.P.: Radiofrequency encoded combinatorial chemistry; Angew. Chem. Int. Ed. Engl. 1995, 34, 2289-2291

  85. Fitch W.; Baer, T.A.; Chen, W.; Holden, F.; Holmes, C.P.; Maclean, D.; Shah, N.; Sullivan, E.; Tang, M.; Waybourn, P.; Fischer, S.M.; Miller, C.A.; Snyder, L.R.: Improved methods for encoding and decoding dialkylamine-encoded combinatorial libraries; J. Comb. Chem. 1999, 1, 188-194

  86. Gillet, V.J.; Willett, P.; Bradshaw, J.: The effectiveness of reactant pools for generating structurally diverse combinatorial libraries; J. Chem. Inf. Comput. Sci. 1997, 37, 731-40

  87. Pivonka, D.E.; Palmer, D.L.: Direct infrared spectroscopic analysis of reagent partitioning in polystyrene bead supported solid phase reaction chemistry; J. Comb. Chem. 1999, 1, 294-296

  88. Chen, X.; Rusinko, A. III; Young, S.S.: Recursive partitioning analysis of a large structure-activity data set using three-dimensional descriptors; J. Chem. Inf. Comput. Sci. 1998, 38, 1054-1062

  89. Young, S.S.; Hawkins, D.M.: Analysis of a 29 full factorial chemical library; J. Med. Chem. 1995, 38, 2784-2788

  90. Rink, H.: Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin; Tetrahedron Lett. 1987, 28, 3787-3790

  91. Lipinski, C.; Lombardo, F.; Dominy, B.W.; Feeney, P.J.: Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings; Adv. Drug. Deliv. Res. 1997, 23, 3-25

  92. Kenner, G.W. Safety catch principle in solid phase peptide synthesis; J. Chem. Soc. D 1971, 636-637

  93. Pátek, M.; Lebl, M.: Safety-catch and multiply cleavable linkers in solid-phase synthesis; Biopolymers 1998, 47, 353-363

  94. Backes, B.J.; Virgilio, A.A.; Ellman, J.A.: Activation method to prepare a highly reactive acylsulfonamide "safety-catch" linker for solid-phase synthesis; J. Am. Chem. Soc. 1996, 118, 3055-3056

  95. Kaldor, S.W.; Siegel, M.G.; Fritz, J.E.; Deressman, B.A.; Hahn, P.J.: Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries; Tetrahedron Lett. 1996, 37, 7193-7196

  96. Booth, R.J.; Hodges, J.C.: Polymer-supported quenching reagents for parallel purification; J. Am. Chem. Soc. 1997, 119, 4882-4886

  97. Flynn, D.L.; Crich, J.Z.; Devraj, R.V.; Hockerman, S.L; Parlow, J.J.; South, M.S.; Woodard, M.S.: Chemical library purification strategies based on principles of complementary molecular reactivity and molecular recognition; J. Am. Chem. Soc. 1997, 119, 4874-4881

  98. Booth R.J.; Hodges, J.C: Solid-supported reagent strategies for rapid purification of combinatorial synthesis products; Acc. Chem. Res. 1999, 32, 18-26.

  99. Parlow, J.J.; Naing, W.; South, M.S.; Flynn, D.L.: In situ chemical tagging: Tetrafluorophthalic anhydride as a "sequestration enabling reagent"in the purification of solution-phase combinatorial libraries; Tetrahedron Lett. 1997, 38, 7959-7962

  100. Winter, M.: Supports for solid-phase organic synthesis, in Combinatorial Peptide and Non-Peptide Libraries; Jung, G., ed.; VCH, Weinheim, 1996

  101. Hudson, D.: Matrix-assisted synthetic transformations: A mosaic of different contributions. 1. The pattern emerges. J. Comb. Chem. 1999, 1, 330-360

  102. Han, H.; Wolfe, M.M.; Brenner, S.; Janda, K.D. Liquid-phase combinatorial synthesis. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 6419-6423

  103. Agrafiotis, D.K.: Stochastic algorithms for maximizing molecular diversity; J. Chem. Inf. Comput. Sci. 1997, 37, 841-851

  104. Freier, S.M.; Konings, D.A.M.; Wyatt, J.R.; Ecker, D,J.: Deconvolution of combinatorial libraries for drug discovery: A model system; J. Med. Chem. 1995, 38, 344-352

  105. Houghten, R.A.: General method for the rapid solid-phase synthesis of large numbers of peptides; Proc. Natl. Acad. Sci. U.S.A. 1985, 82, 5131-5135

  106. Rapp, W.: PEG grafted polystyrene tentacle polymers: Physico-chemical properties and application in chemical synthesis, in Combinatorial Peptide and Non-Peptide Libraries; Jung, G., ed.; VCH, Weinheim 1996, 425-464

  107. Bayer, E.; Towards the chemical synthesis of proteins; Angew. Chem. Int. Ed. Engl. 1991, 30, 113-129

  108. Plunkett, M.J.; Ellman, J.A.: Germanium and silicon linking strategies for traceless solid-phase synthesis; J. Org. Chem. 1997, 62, 2885-2893

  109. Ruhland, T.; Andersen, K.; Pedersen, H.: Selenium-linking strategy for traceless solid-phase synthesis: direct loading, aliphatic C-H bond formation upon cleavage and reaction monitoring by gradient MAS NMR spectroscopy; J. Org. Chem. 1998, 63, 9204-921

  110. Paio, A.; Zaramella, A.; Ferritto, R.; Conti, N.; Marchioro, C.; Seneci, P: Solid-supported benzotriazoles: Synthetic auxiliaries and traceless linkers for the combinatorial synthesis of amine libraries;. J. Comb. Chem. 1999, 1, 317-325

  111. Watters, W.P.; Stahl, M.T.; Murcko, M.A.: Virtual screening — An overview; Drug Discovery Today 1998, 3, 160-178

  112. Wang, S.: p-Alkoxybenzyl alcohol resin and p-alkoxybenzyloxycarbonylhydrazide resin for solid phase synthesis of protected peptide fragements; J. Am. Chem. Soc. 1973, 95, 1328-1333

  113. Yoo S-E.; Gong, Y-D.; Seo, J-S.; Sung, M.M.; Lee, S.S.; Kim, Y.: X-ray photoelectron spectroscopy analysis of solid-phase reactions using 3-brominated Wang resin; J. Comb. Chem. 1999, 1, 177-180

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> References

> Alphabetical Entries

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