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Volumn 6, Issue 1, 2003, Pages 43-53

Catalysis of nucleophilic aromatic substitutions in the 2,6,8-trisubstituted purines and application in the synthesis of combinatorial libraries

Author keywords

Catalysis; Oxidation; Purines; Solid support

Indexed keywords

2,6 DIAMINOPURINE; 2,6 DICHLOROPURINE; POLYMER; POLYSTYRENE; PURINE DERIVATIVE; TRANSITION ELEMENT; UNCLASSIFIED DRUG;

EID: 0042737661     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1024895515316     Document Type: Review
Times cited : (5)

References (58)
  • 2
    • 0034651543 scopus 로고    scopus 로고
    • Whenfold is not important: A common structural framework for adenine and AMP binding in 12 unrelated protein families
    • Denessiouk K. A. and Johnson M. S., Whenfold is not important: a common structural framework for adenine and AMP binding in 12 unrelated protein families, Proteins: Structure, Function, and Genetics, 38 (2000) 310-326.
    • (2000) Proteins: Structure, Function, and Genetics , vol.38 , pp. 310-326
    • Denessiouk, K.A.1    Johnson, M.S.2
  • 3
    • 84979181744 scopus 로고
    • Synthese des hypoxanthins, xanthins, adenins und guanins
    • For instance: a) Fischer, E., Synthese des Hypoxanthins, Xanthins, Adenins und Guanins, Ber., 30 (1887), 2226-2254.
    • (1887) Ber. , vol.30 , pp. 2226-2254
    • Fischer, E.1
  • 4
    • 0041634252 scopus 로고
    • Ueber das oxydichlorpurin
    • b) Fischer, E. and Ach. L., Ueber das Oxydichlorpurin, Ber., 30 (1897) 2208-2219.
    • (1897) Ber. , vol.30 , pp. 2208-2219
    • Fischer, E.1    Ach, L.2
  • 5
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski, C.A., Lombardo, F., Dominy, B.W. and Feeney, P.J., Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings, J. Adv. Drug, Delivery Reviews, 23 (1997) 3-25.
    • (1997) J. Adv. Drug, Delivery Reviews , vol.23 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 6
    • 0034609833 scopus 로고    scopus 로고
    • Fast calculation of molecular polar surface area as a Sum of fragment-based contributions and its application to the prediction of drug transport properties
    • Ertl, P., Rohde, B. and Selzer, P., Fast calculation of molecular polar surface area as a Sum of fragment-based contributions and its application to the prediction of drug transport properties, J. Med. Chem., 43 (2000) 3714-3717.
    • (2000) J. Med. Chem. , vol.43 , pp. 3714-3717
    • Ertl, P.1    Rohde, B.2    Selzer, P.3
  • 7
    • 84956773910 scopus 로고    scopus 로고
    • Library filtering systems and predictions of drug-like properties
    • Walters, W.P. and Murcko, M.A., Library filtering systems and predictions of drug-like properties, Methods Princ. Med. Chem., 10 (2000) 15-32.
    • (2000) Methods Princ. Med. Chem. , vol.10 , pp. 15-32
    • Walters, W.P.1    Murcko, M.A.2
  • 8
    • 0037030707 scopus 로고    scopus 로고
    • Structural classification of protein kinases using 3D molecular interaction field analysis of their ligand binding sites: Target family landscapes
    • Naumann, T. and Matter, H., Structural classification of protein kinases using 3D molecular interaction field analysis of their ligand binding sites: target family landscapes, J. Med. Chem., 45 (2002) 2366-2378.
    • (2002) J. Med. Chem. , vol.45 , pp. 2366-2378
    • Naumann, T.1    Matter, H.2
  • 10
    • 0029090514 scopus 로고
    • Multiple modes of ligand recognition: Crystal structures of cyclin-dependent protein kinase 2 in complex with ATP and two inhibitors, olomoucine and isopentenyladenine
    • Schulze-Gahmen, U., Brandsen, J., Jones, H. D., Morgan, D.O., Meijer, L., Vesely, J. and Kim, S.H., Multiple modes of ligand recognition: crystal structures of cyclin-dependent protein kinase 2 in complex with ATP and two inhibitors, olomoucine and isopentenyladenine, Proteins Struct. Funct. Genet., 22 (1995) 378-391.
    • (1995) Proteins Struct. Funct. Genet. , vol.22 , pp. 378-391
    • Schulze-Gahmen, U.1    Brandsen, J.2    Jones, H.D.3    Morgan, D.O.4    Meijer, L.5    Vesely, J.6    Kim, S.H.7
  • 11
    • 0031028163 scopus 로고    scopus 로고
    • Inhibition of cyclin-dependent kinases by purine analogs. Crystal structure of human cdk2 complexed with roscovitine
    • De Acevedo, W.F., Lecelerc, S., Meijer, L., Havlicek, L., Strnad, M. and Kim, S.H., Inhibition of cyclin-dependent kinases by purine analogs. Crystal structure of human cdk2 complexed with roscovitine, Eur. J. Biochem., 243 (1997) 518-526.
    • (1997) Eur. J. Biochem. , vol.243 , pp. 518-526
    • De Acevedo, W.F.1    Lecelerc, S.2    Meijer, L.3    Havlicek, L.4    Strnad, M.5    Kim, S.H.6
  • 12
    • 0000258537 scopus 로고
    • Base pairing in deoxyribonucleic acid
    • Donohue, J. and Trueblood, K.N., Base pairing in deoxyribonucleic acid, J. Mol. Biol., 2 (1960) 363-371.
    • (1960) J. Mol. Biol. , vol.2 , pp. 363-371
    • Donohue, J.1    Trueblood, K.N.2
  • 13
    • 0002734068 scopus 로고
    • Hydrogen-bonded helical configurations of polynucleotides
    • Donohue, J., Hydrogen-bonded helical configurations of polynucleotides, Proc. Natl. Acad. Sci. USA., 42 (1956) 60-65.
    • (1956) Proc. Natl. Acad. Sci. USA , vol.42 , pp. 60-65
    • Donohue, J.1
  • 17
    • 0029740469 scopus 로고    scopus 로고
    • Structure-based library approach to kinase inhibitors
    • For instance: Norman, T.C., Gray, N. S., Koh, J.T. and Schultz, P.G., Structure-based library approach to kinase inhibitors, J. Am. Chem. Soc., 118 (1996) 7430-7431.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 7430-7431
    • Norman, T.C.1    Gray, N.S.2    Koh, J.T.3    Schultz, P.G.4
  • 18
    • 0035943314 scopus 로고    scopus 로고
    • Synthesis of bicyclic pyrimidine derivatives as ATP analogues
    • For instance: Makara, G.M., Ewing, W., Ma, Y. and Wintner, E. D., Synthesis of bicyclic pyrimidine derivatives as ATP analogues, J. Org. Chem., 66 (2001) 5783-5789.
    • (2001) J. Org. Chem. , vol.66 , pp. 5783-5789
    • Makara, G.M.1    Ewing, W.Ma.Y.2    Wintner, E.D.3
  • 19
    • 0037181078 scopus 로고    scopus 로고
    • A combinatorial approach toward kinase-directed heterocycle libraries
    • Ding, S., Gray, N.S., Wu, X., Ding, Q. and Schultz, P.G., A combinatorial approach toward kinase-directed heterocycle libraries, J. Am. Chem. Soc., 124 (2002) 1594-1596.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1594-1596
    • Ding, S.1    Gray, N.S.2    Wu, X.3    Ding, Q.4    Schultz, P.G.5
  • 20
    • 0036518392 scopus 로고    scopus 로고
    • Resin-capture and release strategy toward combinatorial libraries of 2,6,9-substituted purines
    • Ding, S., Gray, N.S., Ding, Q., Wu, X. and Schultz, P.G., Resin-capture and release strategy toward combinatorial libraries of 2,6,9-substituted purines, J. Comb. Chem., 4 (2002) 183-186.
    • (2002) J. Comb. Chem. , vol.4 , pp. 183-186
    • Ding, S.1    Gray, N.S.2    Ding, Q.3    Wu, X.4    Schultz, P.G.5
  • 21
    • 84889165814 scopus 로고    scopus 로고
    • note
    • We used reaction blocks for parallel chemistry in the standard 96-well format obtained from Robbins Scientific Corp., 1250 Elko Drive, Sunnyvale, CA 94089-2213, USA or Charybdis Technologies, Inc. 5925 Priestly Dr. Carlsbad, CA 92008, USA.
  • 22
    • 0034340226 scopus 로고    scopus 로고
    • Synthesis of acyclic nucleoside and nucleotide analogs derived from 6-amino-7H-purine-8(9H)-thione and 8-(methylsulfanyl)adelzine
    • For instance: Janeba, Z., Holy, A. and Masojidkova, M., Synthesis of acyclic nucleoside and nucleotide analogs derived from 6-amino-7H-purine-8(9H)-thione and 8-(methylsulfanyl)adelzine, Collect. Czech. Chem. Commun. 65, (2000) 1126-1144.
    • (2000) Collect. Czech. Chem. Commun. , vol.65 , pp. 1126-1144
    • Janeba, Z.1    Holy, A.2    Masojidkova, M.3
  • 23
    • 33947480088 scopus 로고
    • 2′-Deoxythioguanosine and related nucleosides
    • Iwamoto, R.H., Acton, E.M. and Goodman, L., 2′-Deoxythioguanosine and related nucleosides, J. Med. Chem., 6 (1963) 684-688.
    • (1963) J. Med. Chem. , vol.6 , pp. 684-688
    • Iwamoto, R.H.1    Acton, E.M.2    Goodman, L.3
  • 24
    • 45949123116 scopus 로고
    • Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin
    • Rink, H., Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin, Tetrahedon Lett., 28 (1987) 3787-3790.
    • (1987) Tetrahedon Lett. , vol.28 , pp. 3787-3790
    • Rink, H.1
  • 25
    • 0002719248 scopus 로고    scopus 로고
    • Immobilizations of nucleophiles on polystyrene supports
    • Brill, W.K.-D., Schmidt, E. and Tommasi, R.A., Immobilizations of nucleophiles on polystyrene supports, Synlett, (1998) 906-908.
    • (1998) Synlett , pp. 906-908
    • Brill, W.K.-D.1    Schmidt, E.2    Tommasi, R.A.3
  • 26
    • 0034935901 scopus 로고    scopus 로고
    • Catalysis of 2-and 6-substitution reactions of purines on solid phase
    • Brill, W.K.-D. Brill, Riva-Toniolo, C. and Mueller, S., Catalysis of 2-and 6-substitution reactions of purines on solid phase, Synlett, 7 (2001) 1097-1100.
    • (2001) Synlett , vol.7 , pp. 1097-1100
    • Brill, W.K.-D.1    Brill Riva-Toniolo, C.2    Mueller, S.3
  • 27
    • 0033613705 scopus 로고    scopus 로고
    • A decarboxylative traceless linker approach for the solid phase synthesis of quinazolines
    • Cobb, J.M., Fiorini, M.T., Goddard, C.R., Theoclitou, M.-E. and Abell, C., A decarboxylative traceless linker approach for the solid phase synthesis of quinazolines, Tetrahedron Lett., 40 (1999) 1045-1048.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1045-1048
    • Cobb, J.M.1    Fiorini, M.T.2    Goddard, C.R.3    Theoclitou, M.-E.4    Abell, C.5
  • 28
    • 0033527607 scopus 로고    scopus 로고
    • NAR-labile linkers: Application to the solid phase synthesis of aminopyridazines
    • NAR-labile linkers: Application to the solid phase synthesis of aminopyridazines, Tetrahedron Lett., 40 (1999) 7975-7978.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 7975-7978
    • Parrot, I.1    Wermuth, C.-G.2    Hibert, M.3
  • 29
    • 0043137086 scopus 로고
    • Heterocyclic basic compounds. VI. Dialkylamino-alkylaminopurines
    • Adams, R. R. and Whitmore, F. C., Heterocyclic basic compounds. VI. Dialkylamino-alkylaminopurines, J. Am., Chem. Soc., 67 (1945) 1271-1273.
    • (1945) J. Am., Chem. Soc. , vol.67 , pp. 1271-1273
    • Adams, R.R.1    Whitmore, F.C.2
  • 30
    • 0042636186 scopus 로고
    • Synthesis of potential anticancer agents. III. Hydrazino analogs of biologically active purines
    • Montgomery, J. A. and Holum, L. B., Synthesis of potential anticancer agents. III. Hydrazino analogs of biologically active purines, J. Am. Chem. Soc., 79 (1957) 2185-2188.
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 2185-2188
    • Montgomery, J.A.1    Holum, L.B.2
  • 31
    • 33947469482 scopus 로고
    • Synthesis of potential anticancer agents. XI. N2,6-Alkyl derivatives of 2,6-diaminopurine
    • Montgomery, J. A. and Holum, L. B., Synthesis of potential anticancer agents. XI. N2,6-Alkyl derivatives of 2,6-diaminopurine, J. Am. Chem. Soc., 80 (1958) 404-408.
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 404-408
    • Montgomery, J.A.1    Holum, L.B.2
  • 33
    • 0001370260 scopus 로고
    • Syntheses of purines. VII. Some transformations of 2,6-dichloro-9-methylpurine
    • Ovcharova, I. M. and Golovchinskaya, E. S., Syntheses of purines. VII. Some transformations of 2,6-dichloro-9-methylpurine, Zh. Obshch. Khim., 34 (1964) 3247-3254.
    • (1964) Zh. Obshch. Khim. , vol.34 , pp. 3247-3254
    • Ovcharova, I.M.1    Golovchinskaya, E.S.2
  • 34
    • 84889164170 scopus 로고    scopus 로고
    • note
    • 1H-NMR and UV-spectral analysis of oxidative degradation products 14a, b, d, g, 16 and comparison with the corresponding starting materials supported assumptions on the location of substituents.
  • 35
    • 0043137103 scopus 로고
    • Electronic structure and spectra of organic molecules. IX. Self-consistent field molecular orbitals configuration interaction calculations for 2,6-disubstituted purines
    • 1H-NMR and UV-spectral analysis of oxidative degradation products 14a, b, d, g, 16 and comparison with the corresponding starting materials supported assumptions on the location of substituents.
    • (1969) Theoretica Chimica Acta , vol.13 , pp. 149-154
    • Kwiatkowski, J.S.1
  • 36
    • 84889120896 scopus 로고    scopus 로고
    • note
    • 1H-NMR and UV-spectral analysis of oxidative degradation products 14a, b, d, g, 16 and comparison with the corresponding starting materials supported assumptions on the location of substituents.
  • 37
    • 0041634250 scopus 로고
    • Correlation of the proton magnetic resonance chemical shifts of substituted purines with reactivity parameters. I. 2,6-Disubstituted purines
    • a) Initial NMR, UV and IR references are: a) Coburn, Jr, W. C., Thorpe, M. C., Montgomery, J. A., Hewson, K., Correlation of the proton magnetic resonance chemical shifts of substituted purines with reactivity parameters. I. 2,6-Disubstituted purines, J. Org. Chem., 30 (1965) 1110-1113.
    • (1965) J. Org. Chem. , vol.30 , pp. 1110-1113
    • Coburn W.C., Jr.1    Thorpe, M.C.2    Montgomery, J.A.3    Hewson, K.4
  • 38
    • 0011816375 scopus 로고
    • Correlation of the proton magnetic resonance chemical shifts of substituted purines with reactivity parameters. II. 6-Substituted purines
    • b) Coburn, Jr, W. C., Thorpe, M. C., Montgomery, J. A. and Hewson, K., Correlation of the proton magnetic resonance chemical shifts of substituted purines with reactivity parameters. II. 6-Substituted purines, J. Org. Chem., 30 (1965) 1114-1117.
    • (1965) J. Org. Chem. , vol.30 , pp. 1114-1117
    • Coburn W.C., Jr.1    Thorpe, M.C.2    Montgomery, J.A.3    Hewson, K.4
  • 39
    • 0035801887 scopus 로고    scopus 로고
    • The bromination of purines with a charge transfer complex between bromine and lutidine
    • Brill, W.K.-D. and Riva-Toniolo, C., The bromination of purines with a charge transfer complex between bromine and lutidine, Tetrahedron Lett., 42 (2002) 6279-6382.
    • (2002) Tetrahedron Lett. , vol.42 , pp. 6279-6382
    • Brill, W.K.-D.1    Riva-Toniolo, C.2
  • 40
    • 0030996347 scopus 로고    scopus 로고
    • Palladium catalyzed amination of aryl chlorides
    • Reddy, N.P. and Tanaka, M., Palladium catalyzed amination of aryl chlorides, Tetrahedron Lett., 38 (1997) 4807-4810.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4807-4810
    • Reddy, N.P.1    Tanaka, M.2
  • 41
    • 0033597748 scopus 로고    scopus 로고
    • Room-temperature palladium-catalyzed amination of aryl bromides and chlorides and extended scope of aromatic C-N bond formation with a commercial ligand
    • Hartwig, J.F., Kawatsura, M., Hauck, S.I., Shaughnessy, K.H. and Alcazar-Roman, L.M. Roman, Luis M., Room-temperature palladium-catalyzed amination of aryl bromides and chlorides and extended scope of aromatic C-N bond formation with a commercial ligand, J. Org. Chem., 64 (1999) 5575-5580.
    • (1999) J. Org. Chem. , vol.64 , pp. 5575-5580
    • Hartwig, J.F.1    Kawatsura, M.2    Hauck, S.I.3    Shaughnessy, K.H.4    Alcazar-Roman, L.M.5    Roman Luis, M.6
  • 42
    • 84889115475 scopus 로고    scopus 로고
    • note
    • Irori Kans™: Discovery Partners International, 9640 Towne Centre Drive San Diego, CA 92121, USA.
  • 44
    • 0031766788 scopus 로고    scopus 로고
    • The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases
    • For instance: Nolsoe, J.M.J., Gundersen, L.-L. and Rise, F., The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases, Synth. Commun., 28, (1998) 4303-4315.
    • (1998) Synth. Commun. , vol.28 , pp. 4303-4315
    • Nolsoe, J.M.J.1    Gundersen, L.-L.2    Rise, F.3
  • 45
    • 0004265358 scopus 로고
    • Ueber adenine und hypoxanthin
    • Bruns, G., Ueber Adenine und Hypoxanthin, Ber. Dtsch. Chem. Ges., 23 (1890) 225-229.
    • (1890) Ber. Dtsch. Chem. Ges. , vol.23 , pp. 225-229
    • Bruns, G.1
  • 47
    • 0019626391 scopus 로고
    • Photopolymerization initiated by charge-transfer complex. I. Photopolymerization of methyl methacrylate with the use of quinaldine-bromine and lutidine-bromine charge-transfer complexes as photoinitiator
    • Mishra, M.K., Lenka, S. and Nayak, P.L., Photopolymerization initiated by charge-transfer complex. I. Photopolymerization of methyl methacrylate with the use of quinaldine-bromine and lutidine-bromine charge-transfer complexes as photoinitiator, J. Polym. Sci., Polym. Chem. Ed., 19 (1981) 2457-2464.
    • (1981) J. Polym. Sci., Polym. Chem. Ed. , vol.19 , pp. 2457-2464
    • Mishra, M.K.1    Lenka, S.2    Nayak, P.L.3
  • 48
    • 0043055689 scopus 로고
    • Ueber die vermeintlichen imid- und amidchloride, die salze der nitrile und saeureamide, sowie ueber den chemismus der umwandlung von nitrilen in saeureamide
    • Hantsch, A., Ueber die vermeintlichen Imid- und Amidchloride, die Salze der Nitrile und Saeureamide, sowie ueber den Chemismus der Umwandlung von Nitrilen in Saeureamide, Ber., 64 (1931) 667-678.
    • (1931) Ber. , vol.64 , pp. 667-678
    • Hantsch, A.1
  • 49
    • 0004262919 scopus 로고
    • Conductances of hydrogen halides in anhydrous polar organic solvents
    • Janz, G.J. and Danyluk, S.S., Conductances of hydrogen halides in anhydrous polar organic solvents, J. Chem. Rev., 60 (1960) 209-234.
    • (1960) J. Chem. Rev. , vol.60 , pp. 209-234
    • Janz, G.J.1    Danyluk, S.S.2
  • 50
    • 0000566751 scopus 로고
    • Nucleophilic attacks on carbon-nitrogen double bonds. Diversity of mechanisms for the substitution of diarylimidoyl chlorides by amines in benzene
    • Ta-Shma, R. and Rappoport, Z., Nucleophilic attacks on carbon-nitrogen double bonds. Diversity of mechanisms for the substitution of diarylimidoyl chlorides by amines in benzene, J. Am. Chem. Soc., 99 (1977) 1845-1858.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 1845-1858
    • Ta-Shma, R.1    Rappoport, Z.2
  • 51
    • 84981838262 scopus 로고
    • Hydrolyse von carbonsaeureimidochloriden
    • Ugi, I., Beck, F. and Fetzer, U., Hydrolyse von Carbonsaeureimidochloriden, Chem Ber., 95 (1962) 126-135.
    • (1962) Chem Ber. , vol.95 , pp. 126-135
    • Ugi, I.1    Beck, F.2    Fetzer, U.3
  • 53
    • 0029063040 scopus 로고
    • On the syntheses of 8-heteroaryl-substituted 9-(β-D-ribofuranosyl)-2,6-diaminopurines through Pd-catalyzed coupling in the presence of cupric oxide
    • Ozola, V., Persson, T., Gronowitz, S. and Hoernfeldt, A.-B., On the syntheses of 8-heteroaryl-substituted 9-(β-D-ribofuranosyl)-2,6-diaminopurines through Pd-catalyzed coupling in the presence of cupric oxide, J. Heterocycl. Chem., 32 (1995) 863-866.
    • (1995) J. Heterocycl. Chem. , vol.32 , pp. 863-866
    • Ozola, V.1    Persson, T.2    Gronowitz, S.3    Hoernfeldt, A.-B.4
  • 54
    • 0035840343 scopus 로고    scopus 로고
    • Solid phase synthesis of 2,6,8-trisubstituted purines
    • Brill, W.K.-D. and Riva-Toniolo, C., Solid phase synthesis of 2,6,8-trisubstituted purines, Tetrahedron Lett., 42 (2001) 6515-6518.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6515-6518
    • Brill, W.K.-D.1    Riva-Toniolo, C.2
  • 55
    • 0028815228 scopus 로고
    • Radio frequency tag encoded combinatorial library method for the discovery of tripeptide-substituted cinnamic acid inhibitors of the protein tyrosine phosphatase PTP1B
    • Moran, E.J., Sarshar, S., Cargill, J.F., Shahbaz, M.M., Lio, A., Mjalli, A.M.M. and Armstrong, R.W., Radio frequency tag encoded combinatorial library method for the discovery of tripeptide-substituted cinnamic acid inhibitors of the protein tyrosine phosphatase PTP1B, J. Am. Chem. Soc., 117 (1995) 10787-10788.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10787-10788
    • Moran, E.J.1    Sarshar, S.2    Cargill, J.F.3    Shahbaz, M.M.4    Lio, A.5    Mjalli, A.M.M.6    Armstrong, R.W.7
  • 56
    • 0025893762 scopus 로고
    • General method for rapid synthesis of multicomponent peptide mixtures
    • Furka, A., Sebestyen, F., Asgedom, M. and Dibo, G., General method for rapid synthesis of multicomponent peptide mixtures, Int. J. Pept. Protein Res., 37 (1991) 487-493.
    • (1991) Int. J. Pept. Protein Res. , vol.37 , pp. 487-493
    • Furka, A.1    Sebestyen, F.2    Asgedom, M.3    Dibo, G.4
  • 57
    • 0031960506 scopus 로고    scopus 로고
    • A visual tagging process for mix and sort combinatorial chemistry
    • Guiles, J.W., Lanter, C.L. and Rivero, R.A., A visual tagging process for mix and sort combinatorial chemistry, Angew. Chem. Int. Ed., 37 (1998) 926-928.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 926-928
    • Guiles, J.W.1    Lanter, C.L.2    Rivero, R.A.3
  • 58
    • 0032559294 scopus 로고    scopus 로고
    • Automated analytical/preparative high-performance liquid chromatography-mass spectrometry system for the rapid characterization and purification of compound libraries
    • For instance: Zeng, L., Burton, L., Yung, K., Shushan, B. and Kassel, D.B., Automated analytical/preparative high-performance liquid chromatography-mass spectrometry system for the rapid characterization and purification of compound libraries, J. Chromatography A, 794 (1998) 3-13.
    • (1998) J. Chromatography A , vol.794 , pp. 3-13
    • Zeng, L.1    Burton, L.2    Yung, K.3    Shushan, B.4    Kassel, D.B.5


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