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Volumn 3, Issue 2, 1997, Pages 95-112

Solid-supported syntheses of 3-thio-1,2,4-triazoles

Author keywords

1,2,4 triazole; Combinatorial library; Molecular similarity; Parallel synthesis; Solid supported synthesis; Tanimoto coefficient

Indexed keywords

AMINO ACID; FLUORENE DERIVATIVE; FORMIC ACID DERIVATIVE; HETEROCYCLIC COMPOUND; N(ALPHA) FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS; N(ALPHA)-FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS; RESIN; RINK AMIDE RESIN; T BUTYLOXYCARBONYL GROUP; T-BUTYLOXYCARBONYL GROUP; THIOL DERIVATIVE; TRIAZOLE DERIVATIVE;

EID: 0031995222     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1023/a:1009696119443     Document Type: Article
Times cited : (17)

References (27)
  • 1
    • 0028243847 scopus 로고
    • Applications of combinatorial technologies to drug discovery. 1. Background and peptide combinatorial libraries
    • a. Gallop, M.A., Barrett, R.W., Dower, W.J., Fodor, S.P.A. and Gordon, E.M., Applications of combinatorial technologies to drug discovery. 1. Background and peptide combinatorial libraries, J. Med. Chem., 9 (1994) 1233-1251.
    • (1994) J. Med. Chem. , vol.9 , pp. 1233-1251
    • Gallop, M.A.1    Barrett, R.W.2    Dower, W.J.3    Fodor, S.P.A.4    Gordon, E.M.5
  • 2
    • 0028318863 scopus 로고
    • Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions
    • b. Gordon, E.M., Barrett, R.W., Dower, W.J., Fodor, S.P.A. and Gallop, M.A., Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions, J. Med. Chem., 10 (1994) 1386-1401.
    • (1994) J. Med. Chem. , vol.10 , pp. 1386-1401
    • Gordon, E.M.1    Barrett, R.W.2    Dower, W.J.3    Fodor, S.P.A.4    Gallop, M.A.5
  • 3
    • 0041166277 scopus 로고
    • Combinatorial organic libraries
    • c. Ellman, J.A., Combinatorial organic libraries, Chemtracts Org. Chem., 8 (1995) 1-4.
    • (1995) Chemtracts Org. Chem. , vol.8 , pp. 1-4
    • Ellman, J.A.1
  • 4
    • 0041445345 scopus 로고
    • Combinatorial libraries: Chemistry meets Darwin
    • d. Pirrung, M.C., Combinatorial libraries: Chemistry meets Darwin, Chemtracts Org. Chem., 8 (1995) 5-12.
    • (1995) Chemtracts Org. Chem. , vol.8 , pp. 5-12
    • Pirrung, M.C.1
  • 5
    • 0001926616 scopus 로고
    • Why combinatorial chemistry, why now (and why you should care)
    • e. Czarnik, A.W., Why combinatorial chemistry, why now (and why you should care), Chemtracts Org. Chem., 8 (1995) 13-18.
    • (1995) Chemtracts Org. Chem. , vol.8 , pp. 13-18
    • Czarnik, A.W.1
  • 6
    • 0010327365 scopus 로고
    • Some ruminations on the present and future roles of combinatorial and multiplex syntheses in medicinal chemistry
    • f. Mitscher, L.A., Some ruminations on the present and future roles of combinatorial and multiplex syntheses in medicinal chemistry, Chemtracts Org. Chem., 8 (1995) 19-25.
    • (1995) Chemtracts Org. Chem. , vol.8 , pp. 19-25
    • Mitscher, L.A.1
  • 7
    • 0344745897 scopus 로고
    • Triazoles, 1, 2, 4
    • Montgomery, J.A. (Ed.) Wiley, New York, NY
    • Temple Jr., C., Triazoles, 1, 2, 4, In Montgomery, J.A. (Ed.) The Chemistry of Heterocyclic Compounds, Vol. 37, Wiley, New York, NY, 1981, pp. 251-287.
    • (1981) The Chemistry of Heterocyclic Compounds , vol.37 , pp. 251-287
    • Temple Jr., C.1
  • 9
    • 0030943408 scopus 로고    scopus 로고
    • Selecting optimally diverse compounds from structured databases: A validation study of two-dimensional and three-dimensional molecular descriptors
    • and references therein
    • a. Matter, H., Selecting optimally diverse compounds from structured databases: A validation study of two-dimensional and three-dimensional molecular descriptors, J. Med. Chem., 40 (1997) 1219-1229, and references therein.
    • (1997) J. Med. Chem. , vol.40 , pp. 1219-1229
    • Matter, H.1
  • 10
    • 0022620276 scopus 로고
    • A comparison of some measures for the determination of intermolecular structural similarity
    • and references therein
    • b. Willett, P. and Winterman, V., A comparison of some measures for the determination of intermolecular structural similarity, Quant. Struct.-Act. Relatsh., 5 (1986) 18-25, and references therein.
    • (1986) Quant. Struct.-Act. Relatsh. , vol.5 , pp. 18-25
    • Willett, P.1    Winterman, V.2
  • 12
    • 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, Tetrahedron Lett., 28 (1987) 3787-3790.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 3787-3790
    • Rink, H.1
  • 13
    • 0038145589 scopus 로고    scopus 로고
    • Solid-supported tert-alkoxycarbonylation reagents for anchoring of amines during solid-phase organic synthesis
    • Hernández, A.S. and Hodges, J.C., Solid-supported tert-alkoxycarbonylation reagents for anchoring of amines during solid-phase organic synthesis, J. Org. Chem., 62 (1997) 3153-3157.
    • (1997) J. Org. Chem. , vol.62 , pp. 3153-3157
    • Hernández, A.S.1    Hodges, J.C.2
  • 14
    • 33947461923 scopus 로고
    • Preparation of some derivatives of β-(10-phenothiazinyl) propionic acid and β-(2-chloro-10-phenothiazinyl) propionic acid
    • Godefroi, E.F. and Wittle, E.L., Preparation of some derivatives of β-(10-phenothiazinyl) propionic acid and β-(2-chloro-10-phenothiazinyl) propionic acid, J. Org. Chem., 21 (1956) 1163-1168.
    • (1956) J. Org. Chem. , vol.21 , pp. 1163-1168
    • Godefroi, E.F.1    Wittle, E.L.2
  • 16
    • 0000429154 scopus 로고
    • Cycloadditions. XI. Cycloaddition of diphenylketene to some C=N heterocycles. Structural assignment and reactions of adducts
    • Haddadin, M.J. and Hassner, A., Cycloadditions. XI. Cycloaddition of diphenylketene to some C=N heterocycles. Structural assignment and reactions of adducts, J. Org. Chem., 15 (1973) 2650-2652.
    • (1973) J. Org. Chem. , vol.15 , pp. 2650-2652
    • Haddadin, M.J.1    Hassner, A.2
  • 18
    • 0028956786 scopus 로고
    • A strategy of urea linked diamine libraries
    • Hutchins, S.M. and Chapman, K.T., A strategy of urea linked diamine libraries, Tetrahedron Lett., 36 (1995) 2583-2586.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2583-2586
    • Hutchins, S.M.1    Chapman, K.T.2
  • 19
    • 0000303126 scopus 로고
    • Di-2-pyridyl thionocarbonate. A new reagent for the preparation of isothiocyanates and carbodiimides
    • a. Kim, S. and Yi, K.Y., Di-2-pyridyl thionocarbonate. A new reagent for the preparation of isothiocyanates and carbodiimides, Tetrahedron Lett., 26 (1985) 1661-1664.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 1661-1664
    • Kim, S.1    Yi, K.Y.2
  • 20
    • 33845374357 scopus 로고
    • 1,1′-Thiocarbonyldi-2,2′-pyridone. a new useful reagent for functional group conversions under essentially neutral conditions
    • b. Kim, S. and Yi, K.Y., 1,1′-Thiocarbonyldi-2,2′-pyridone. A new useful reagent for functional group conversions under essentially neutral conditions, J. Org. Chem., 3 (1986) 2613-2615.
    • (1986) J. Org. Chem. , vol.3 , pp. 2613-2615
    • Kim, S.1    Yi, K.Y.2
  • 21
    • 2342601104 scopus 로고    scopus 로고
    • SYBYL, Tripos Inc., St. Louis, MO, U.S.A.
    • SYBYL, Tripos Inc., St. Louis, MO, U.S.A.
  • 22
    • 0345154742 scopus 로고
    • Libraries from libraries: The generation of peptidomimetic combinatorial diversities
    • Maia, H.L.S. (Ed.) Peptides 1994 ESCOM, Leiden
    • Houghten, R.A., Ostresh, J.M., Husar, G.M., Dorner, B. and Blondelle, S.E., Libraries from libraries: The generation of peptidomimetic combinatorial diversities, In Maia, H.L.S. (Ed.) Peptides 1994 (Proceedings of the 23rd European Peptide Symposium), ESCOM, Leiden, 1995, pp. 459-460.
    • (1995) Proceedings of the 23rd European Peptide Symposium , pp. 459-460
    • Houghten, R.A.1    Ostresh, J.M.2    Husar, G.M.3    Dorner, B.4    Blondelle, S.E.5
  • 23
    • 0030607141 scopus 로고    scopus 로고
    • Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries
    • a. Kaldor, S.W., Siegel, M.G., Fritz, J.E., Dressman, B.A. and Hahn, P.J., Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries, Tetrahedron Lett., 37 (1996) 7193-7196.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7193-7196
    • Kaldor, S.W.1    Siegel, M.G.2    Fritz, J.E.3    Dressman, B.A.4    Hahn, P.J.5
  • 24
    • 0030591840 scopus 로고    scopus 로고
    • Discovery of antirhinoviral leads by screening a combinatorial library of ureas prepared using covalent scavengers
    • b. Kaldor, S.W., Fritz, J.E., Tang, K. and McKinney, E.R., Discovery of antirhinoviral leads by screening a combinatorial library of ureas prepared using covalent scavengers, Bioorg. Med. Chem. Lett., 24 (1996) 3041-3044.
    • (1996) Bioorg. Med. Chem. Lett. , vol.24 , pp. 3041-3044
    • Kaldor, S.W.1    Fritz, J.E.2    Tang, K.3    McKinney, E.R.4
  • 25
    • 0030987922 scopus 로고    scopus 로고
    • Polymer-supported quenching reagents for parallel purification
    • c. Booth, R.J. and Hodges, J.C., Polymer-supported quenching reagents for parallel purification, J. Am. Chem. Soc., 119 (1997) 4882-4886.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4882-4886
    • Booth, R.J.1    Hodges, J.C.2
  • 26
    • 0030952762 scopus 로고    scopus 로고
    • Chemical library purification strategies based on principles of complementary molecular reactivity and molecular recognition
    • d. Flynn, D.L., Crich, J.Z., Devraj, R.V., Hockerman, S.L., Parlow, J.J. and South, M.S., Chemical library purification strategies based on principles of complementary molecular reactivity and molecular recognition, J. Am. Chem. Soc., 119 (1997) 4874-4881.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4874-4881
    • Flynn, D.L.1    Crich, J.Z.2    Devraj, R.V.3    Hockerman, S.L.4    Parlow, J.J.5    South, M.S.6
  • 27
    • 0005689810 scopus 로고    scopus 로고
    • Compound libraries for lead discovery
    • Matter, H. and Lassen, F., Compound libraries for lead discovery, Chim. Oggi, 14 (1996) 9-15.
    • (1996) Chim. Oggi , vol.14 , pp. 9-15
    • Matter, H.1    Lassen, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.