News
& Notices
Organizations & People
Standing
Committees
Divisions
Projects
Reports
..By Year
..By Division
..Other Committees
..Provisionals
Publications
Symposia
AMP
Links
of Interest
Search
the Site
Home
Page
|
|
Pure Appl. Chem.,
Vol. 71, No. 12, pp. 2349-2365, 1999
Glossary of Terms Used in Combinatorial
Chemistry
[A-B]
[C] [D] [E-G]
[H-K] [L]
[M-N] [O-P] [Q] [R]
[S] [T] [U-Z]
References:
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
-
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
-
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
-
Tuerk, C., Gold, L.: Systematic evolution of ligands
by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase;
Science 1990, 249, 505-510
-
Ellington, A.D., Szostak, J.W.: In vitro
selection of RNA molecules that bind specific ligands; Nature
1990, 346, 818-822
-
Osborne, S.E.; Ellington, A.D.: Nucleic acid selection
and the challenge of combinatorial chemistry; Chem. Rev. 1997,
97, 349-370
-
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
-
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
-
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
-
Pirrung, M.C.: Spatially addressable combinatorial
libraries; Chem. Rev. 1997, 97, 473-488
-
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
-
Martin, E.J.; Critchlow, R.E.: Beyond mere diversity:
tailoring combinatorial libraries for drug discovery; J. Comb.
Chem. 1999, 1, 32-45
-
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
-
Instructions to Authors, J. Comb. Chem.
1999, 1, 11A
-
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
-
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
-
Gorse, D.; Rees, A.; Kaczorek, M.; Lahana, R.:
Molecular diversity and its analysis; Drug Discovery Today
1999, 4, 257-264
-
Sherrington, D.C.: Preparation, structure, and
morphology of polymer supports; Chem. Commun. 1998,
2275-2286
-
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
-
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
-
Czarnik, A.W.: Encoding methods for combinatorial
chemistry; Curr. Opin. Chem. Biol. 1997, 1,
60-66
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
Spaller, M.R.; Burger, M.T.; Fardis, M.; Bartlett,
P.A.: Synthetic strategies in combinatorial chemistry; Curr.
Opin. Chem. Biol. 1997, 1, 47-53
-
Baldwin, J.J.; Horlbeck, E.G.: Synthesis of combinatorial
libraries; U.S. Patent 5,663,046
-
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
-
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
-
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
-
Ganesan A.: Strategies for the dynamic integration
of combinatorial synthesis and screening; Angew. Chem. Intl.
Ed. 1998, 37, 2828-2831
-
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
-
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
-
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
-
Hird, N.W.: Automated synthesis: New tools for
the organic chemist; Drug Discovery Today 1999, 4,
265-274
-
Curran, D.P.: Strategy-level separation in organic
synthesis: From planning to practice; Angew. Chem. Int. Ed.
1998, 37, 1174-1196
-
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
-
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
-
Ellman, J.A.: Design, synthesis, and evaluation
of small-molecule libraries; Acc. Chem. Res. 1996,
29, 132-143
-
Weber, L.: Applications of genetic algorithms
in molecular diversity; Curr. Opin. Chem. Biol. 1998,
2, 381-385
-
Sheridan, R.P.; Kearsley, S.K.: Using a genetic
algorithm to suggest combinatorial libraries; J. Chem. Inf. Comput.
Sci. 1995, 35, 310-320
-
Willett, P.: Genetic algorithms in molecular recognition
and design; Trends Biotech. 1995, 13, 516-521
-
Dove, A.: Drug screening Beyond the bottleneck;
Nature Biotech. 1999, 17, 859-863
-
Taylor, S.J.; Morken, J.P.: Thermographic selection
of effective catalysts from an encoded polymer-bound library; Science
1998, 280, 267-270
-
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
-
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
-
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
-
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
-
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
-
Backes, B.J.; Ellman, J.A.: Solid support linker
strategies; Curr. Opinion. Chem. Biol. 1997, 1,
86-93
-
Bayer, E.; Mutter, M.: Liquid phase synthesis
of peptides; Nature (London) 1972, 237, 512-513
-
Gravert, D.J.; Janda, K.D.: Organic synthesis
on soluble polymer supports: Liquid phase methodologies; Chem.
Rev. 1997, 97, 489-510
-
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
-
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
-
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
-
Merrifield, R.B.: Solid-Phase Peptide Synthesis.
1. The synthesis of a tetrapeptide; J. Am. Chem. Soc. 1963,
85, 2149-2154
-
Gasteiger, J.; Zupan, J.: Neural networks for
chemists: An introduction. VCH, Weinheim, 1993
-
Gasteiger, J.; Zupan, J.: Neural networks in chemistry;
Angew. Chem. Int. Ed. Engl. 1993, 32, 503-527
-
Furka, A.: Sub-library composition of peptide
libraries: potential application in screening; Drug Dev. Res.
1994, 33, 90-97
-
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
-
Déprez, B.; Williard, X.; Bourel, L.; Coste,
H.; Hyafil, F.; Tartar, A.: Orthogonal combinatorial chemical libraries;
J. Am. Chem. Soc. 1995, 117, 5405-5406
-
Erb, E.; Janda, K.D.; Brenner, S.: Recursive deconvolution
of combinatorial chemical libraries. Proc. Natl. Acad. Sci. U.S.A.
1994, 91, 11422-11426
-
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
-
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
-
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
-
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
-
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
-
Scott, J.K.; Smith, G.P.: Searching for peptide
ligands with an epitope library; Science 1990, 249,
386-390
-
Smith, G.P.; Petrenko, V.A.: Phage display; Chem.
Rev. 1997, 97, 391-410
-
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
-
Wermuth, C.; Langer, T.: Pharmacophore identification.
In 3D QSAR in Drug Design; Kubinyi, H. ed.; Escom, Leiden.
1998, 117-136
-
Furka, A.; Bennett, W.D.: Combinatorial libraries
by portioning and mixing; Comb. Chem. High Throughput Screening
1999, 2, 105-122
-
Lam, K.S.; Lebl, M.; KrchHák, V.:
The "one-bead-one-compound" combinatorial library method;
Chem. Rev. 1997, 97, 411-448
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
Young, S.S.; Hawkins, D.M.: Analysis of a 29
full factorial chemical library; J. Med. Chem. 1995,
38, 2784-2788
-
Rink, H.: Solid-phase synthesis of protected peptide
fragments using a trialkoxy-diphenyl-methylester resin; Tetrahedron
Lett. 1987, 28, 3787-3790
-
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
-
Kenner, G.W. Safety catch principle in solid phase
peptide synthesis; J. Chem. Soc. D 1971, 636-637
-
Pátek, M.; Lebl, M.: Safety-catch and multiply
cleavable linkers in solid-phase synthesis; Biopolymers 1998,
47, 353-363
-
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
-
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
-
Booth, R.J.; Hodges, J.C.: Polymer-supported quenching
reagents for parallel purification; J. Am. Chem. Soc. 1997,
119, 4882-4886
-
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
-
Booth R.J.; Hodges, J.C: Solid-supported reagent
strategies for rapid purification of combinatorial synthesis products;
Acc. Chem. Res. 1999, 32, 18-26.
-
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
-
Winter, M.: Supports for solid-phase organic
synthesis, in Combinatorial Peptide and Non-Peptide Libraries;
Jung, G., ed.; VCH, Weinheim, 1996
-
Hudson, D.: Matrix-assisted synthetic transformations:
A mosaic of different contributions. 1. The pattern emerges. J.
Comb. Chem. 1999, 1, 330-360
-
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
-
Agrafiotis, D.K.: Stochastic algorithms for maximizing
molecular diversity; J. Chem. Inf. Comput. Sci. 1997,
37, 841-851
-
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
-
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
-
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
-
Bayer, E.; Towards the chemical synthesis of
proteins; Angew. Chem. Int. Ed. Engl. 1991, 30,
113-129
-
Plunkett, M.J.; Ellman, J.A.: Germanium and silicon
linking strategies for traceless solid-phase synthesis; J. Org.
Chem. 1997, 62, 2885-2893
-
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
-
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
-
Watters, W.P.; Stahl, M.T.; Murcko, M.A.: Virtual
screening An overview; Drug Discovery Today 1998,
3, 160-178
-
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
-
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
> Introduction
> Notes
> References
> Alphabetical
Entries
[A-B]
[C] [D] [E-G]
[H-K] [L]
[M-N] [O-P] [Q] [R]
[S] [T] [U-Z]
Page last modified 10 November 2000.
Copyright © 2000 International Union of Pure and Applied Chemistry.
Questions or comments about IUPAC, please contact, the Secretariat.
Questions regarding the website, please contact Web
Help.
|