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Volumn 13, Issue 11, 2007, Pages 3026-3038

Novel structural motifs consisting of chiral thiazolines: Synthesis, molecular recognition, and anticancer activity

Author keywords

Anticancer agents; Macrocycles; Molecular recognition; Oligomerization; Thiazolines

Indexed keywords

CELL GROWTH; CONDENSATION; MOLECULAR RECOGNITION; MOLECULAR STRUCTURE; OLIGOMERIZATION; OLIGOMERS; SYNTHESIS (CHEMICAL);

EID: 34250668246     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200601446     Document Type: Article
Times cited : (37)

References (36)
  • 3
    • 12044259565 scopus 로고
    • 383; for representative recent research articles on molecular recognition, see
    • c) T. H. Webb, C. S. Wilcox, Chem. Soc. Rev. 1993, 22, 383; for representative recent research articles on molecular recognition, see:
    • (1993) Chem. Soc. Rev , vol.22
    • Webb, T.H.1    Wilcox, C.S.2
  • 8
    • 0002843503 scopus 로고    scopus 로고
    • Eds, J. L. Atwood, J. E. D. Davies, D.D. MacNicol, F. Vogtle, Pergamon Press, Oxford
    • J. Breitenbach, J. Boosfeld, F. Vogtle in Comprehensive Supramolecular Chemistry, Vol. 2 (Eds.: J. L. Atwood, J. E. D. Davies, D.D. MacNicol, F. Vogtle), Pergamon Press, Oxford, 1996, p. 29.
    • (1996) Comprehensive Supramolecular Chemistry , vol.2 , pp. 29
    • Breitenbach, J.1    Boosfeld, J.2    Vogtle, F.3
  • 17
    • 0037159708 scopus 로고    scopus 로고
    • Examples of other approaches to the synthesis of linear arrays of polythiazolines: for mirabazole, see: a
    • Examples of other approaches to the synthesis of linear arrays of polythiazolines: for mirabazole, see: a) B. L. Kedrowski, C. H. Heathcock, Heterocycles 2002, 56, 601;
    • (2002) Heterocycles , vol.56 , pp. 601
    • Kedrowski, B.L.1    Heathcock, C.H.2
  • 26
    • 34250660633 scopus 로고    scopus 로고
    • Crystal data for 30·(CHCl3)2 at 153 K: C34H42Cl6N8S8, M r 1031.99. 0.72×0.52×0.22 mm3, colorless crystal, triclinic. space group P1, a, 8.8700(4, b, 12.0090(9, c, 12.7400(9) Å. α, 116.29(3, β= 88.97(5, γ, 101.44(5)°, V, 1189(13) Å3, Z, 1, final R1 =0.0472 for 3918 reflections on I>2σI, R1, 0.0474, wR2, 0.1262 for all 3918 reflections. CCDC-290621 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via
    • 2 = 0.1262 for all 3918 reflections. CCDC-290621 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 27
    • 34250665913 scopus 로고    scopus 로고
    • 13C NMR spectra of the macrocyclic compounds, see the Supporting Information in reference [9].
    • 13C NMR spectra of the macrocyclic compounds, see the Supporting Information in reference [9].
  • 29
    • 0037136508 scopus 로고    scopus 로고
    • For selected reviews on artificial receptors for carboxylic acids, see reference [1a]; for selected examples of the chiral recognition of mandelic acid, see: b J. Lin, H. C. Zhang, L. Pu, Org. Lett. 2002, 4, 3297;
    • a) For selected reviews on artificial receptors for carboxylic acids, see reference [1a]; for selected examples of the chiral recognition of mandelic acid, see: b) J. Lin, H. C. Zhang, L. Pu, Org. Lett. 2002, 4, 3297;
  • 32
    • 17044377598 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1690.
    • (2005) Chem. Int. Ed , vol.44 , pp. 1690
    • Angew1
  • 33
    • 34250672076 scopus 로고    scopus 로고
    • Extensive studies show evidence that multipoint interactions between a receptor and guest is key to obtaining good enantiomeric recognition because multipoint interactions increase the rigidity of the complex. For a detailed review, see p. 3318 of reference [1b
    • Extensive studies show evidence that multipoint interactions between a receptor and guest is key to obtaining good enantiomeric recognition because multipoint interactions increase the rigidity of the complex. For a detailed review, see p. 3318 of reference [1b].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.