메뉴 건너뛰기




Volumn 3256, Issue , 2004, Pages 83-95

The potential of a chemical graph transformation system

Author keywords

[No Author keywords available]

Indexed keywords

SPECIFICATION LANGUAGES;

EID: 33750257113     PISSN: 03029743     EISSN: 16113349     Source Type: Book Series    
DOI: 10.1007/978-3-540-30203-2_8     Document Type: Article
Times cited : (12)

References (23)
  • 2
    • 0006916971 scopus 로고
    • Subgraph isomorphism in polynomial time
    • University of Bern, Institute of Computer Science and Applied Mathematics
    • Messmer, B.T., Bunke, H.: Subgraph isomorphism in polynomial time. Technical Report IAM 95-003, University of Bern, Institute of Computer Science and Applied Mathematics (1995)
    • (1995) Technical Report IAM 95-003
    • Messmer, B.T.1    Bunke, H.2
  • 3
    • 0002690545 scopus 로고    scopus 로고
    • Automorphism partitioning, and canonical labeling can be solved in polynomial- Time for molecular graphs
    • Faulon, J.L.: Automorphism partitioning, and canonical labeling can be solved in polynomial- time for molecular graphs. Journal of Chemical Information and Computer Sciences 38 (1998) 432-444
    • (1998) Journal of Chemical Information and Computer Sciences , vol.38 , pp. 432-444
    • Faulon, J.L.1
  • 4
    • 0043143008 scopus 로고
    • Algebraic combinatorics in mathematical chemistry. Methods and algorithms. I. Permutation groups and coherent (cellular) algebras
    • Techn. Univ. München
    • Klin, M., Rücker, C., Rücker, G., Tinhofer, G.: Algebraic combinatorics in mathematical chemistry. Methods and algorithms. I. Permutation groups and coherent (cellular) algebras. Technical Report TUM M9510, Techn. Univ. München (1995)
    • (1995) Technical Report TUM M9510
    • Klin, M.1    Rücker, C.2    Rücker, G.3    Tinhofer, G.4
  • 5
    • 0030027833 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant gram-positive bacterial infections
    • Brickner, S.J., et al.: Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant gram-positive bacterial infections. Journal of Medicinal Chemistry 39 (1996) 673-679
    • (1996) Journal of Medicinal Chemistry , vol.39 , pp. 673-679
    • Brickner, S.J.1
  • 6
    • 35048847735 scopus 로고
    • Are you ready for chemical linguistics? Chemical semantics? Chemical semiotics? Or, why WLN?
    • Paper available at: http://www.garfield.library.upenn.edu/essays/ V1p386y1962-73.pdf.
    • Garfield, E.: Are you ready for chemical linguistics? Chemical semantics? Chemical semiotics? Or, why WLN? Essays of an Information Scientist 1 (1972) 386-388 Paper available at: http://www.garfield.library.upenn.edu/essays/ V1p386y1962-73.pdf.
    • (1972) Essays of An Information Scientist , vol.1 , pp. 386-388
    • Garfield, E.1
  • 7
    • 14344281952 scopus 로고
    • Chemico-linguistics: Computer translation of chemical nomenclature
    • Paper avilable at
    • Garfield, E.: Chemico-linguistics: Computer translation of chemical nomenclature. Nature 192 (1961) 192 Paper avilable at: http://www.garfield. library.upenn.edu/essays/v6p489y1983.pdf.
    • (1961) Nature , vol.192 , pp. 192
    • Garfield, E.1
  • 8
    • 0023965741 scopus 로고    scopus 로고
    • SMILES, a chemical language and information-system. 1. Introduction to methodlogy and encoding rules
    • Weininger, D.: SMILES, a chemical language and information-system. 1. Introduction to methodlogy and encoding rules. Journal of Chemical Information and Computer Sciences 28 (1998) 31-36
    • (1998) Journal of Chemical Information and Computer Sciences , vol.28 , pp. 31-36
    • Weininger, D.1
  • 10
    • 0037404132 scopus 로고    scopus 로고
    • Graph canonicalization
    • Kelley, B.P.: Graph canonicalization. Dr. Dobb's Journal 28 (2003) 66-69
    • (2003) Dr. Dobb's Journal , vol.28 , pp. 66-69
    • Kelley, B.P.1
  • 11
    • 0004117251 scopus 로고    scopus 로고
    • Daylight Chemical Information Systems Inc.: (Daylight theory manual) Available at http://www.daylight.com/dayhtml/doc/theory/theory.toc.html.
    • Daylight Theory Manual
  • 12
    • 0026529512 scopus 로고
    • Lewis acid catalyzed Diels-Alder reactions of S-(+)-carvone with silyloxy dienes. Total synthesis of (+)-small alpha, greek-cyperone
    • Haaksna, A.A., Jansen, B.J.M., de Groot, A.: Lewis acid catalyzed Diels-Alder reactions of S-(+)-carvone with silyloxy dienes. Total synthesis of (+)-small alpha, greek-cyperone. Tetrahedron 48 (1992) 3121-3130
    • (1992) Tetrahedron , vol.48 , pp. 3121-3130
    • Haaksna, A.A.1    Jansen, B.J.M.2    De Groot, A.3
  • 15
    • 5244229552 scopus 로고
    • Starting material oriented retrosynthetic analysis in the LHASA program. 2. Mapping the SM and target structures
    • Johnson, A., Marshall, C.: Starting material oriented retrosynthetic analysis in the LHASA program. 2. Mapping the SM and target structures. Journal of Chemical Information and Computer Sciences 32 (1992) 418-425
    • (1992) Journal of Chemical Information and Computer Sciences , vol.32 , pp. 418-425
    • Johnson, A.1    Marshall, C.2
  • 16
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • Rostovtsev, V.V., Green, L.G., Fokin, V.V., Sharpless, K.B.: A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angewandte Chemie International Edition 41 (2002) 2596-2599
    • (2002) Angewandte Chemie International Edition , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 17
    • 0030039619 scopus 로고    scopus 로고
    • The art and practice of structure-based drug design: A molecular modeling perspective
    • Bohacek, U.S., McMartin, C., Guida, W.C.: The art and practice of structure-based drug design: A molecular modeling perspective. Medicinal Research Reviews 16 (1998) 3-50
    • (1998) Medicinal Research Reviews , vol.16 , pp. 3-50
    • Bohacek, U.S.1    McMartin, C.2    Guida, W.C.3
  • 18
    • 0031320340 scopus 로고    scopus 로고
    • Autocatalytic networks: The transition from molecular self-replication to molecular ecosystems
    • Lee, D.H., Severin, K., Ghadiri, M.R.: Autocatalytic networks: The transition from molecular self-replication to molecular ecosystems. Current Opinion in Chemical Biology 1 (1997) 491-496
    • (1997) Current Opinion in Chemical Biology , vol.1 , pp. 491-496
    • Lee, D.H.1    Severin, K.2    Ghadiri, M.R.3
  • 20
    • 0035799707 scopus 로고    scopus 로고
    • Lethality and centrality in protein networks
    • Jeong, H., Mason, S., Barabási, A.L., Oltvai, N.Z.: Lethality and centrality in protein networks. Nature 411 (2001) 41-42
    • (2001) Nature , vol.411 , pp. 41-42
    • Jeong, H.1    Mason, S.2    Barabási, A.L.3    Oltvai, N.Z.4
  • 21
    • 0141757360 scopus 로고    scopus 로고
    • Life and the art of networks
    • Ray, L.B., Jansy, B.R.: Life and the art of networks. Science 301 (2003) 1863
    • (2003) Science , vol.301 , pp. 1863
    • Ray, L.B.1    Jansy, B.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.