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Volumn 44, Issue 49, 2003, Pages 8801-8804

Synthesis and anion recognition properties of 8,8′-dithioureido-2, 2′-binaphthalene

Author keywords

2,2 binaphthalene; Anion recognition; Hydrogen bond; Thiourea

Indexed keywords

8,8' DITHIOUREIDO 2,2' BINAPHTHALENE; ACETONITRILE; ANION; BROMIDE; NAPHTHALENE DERIVATIVE; NICKEL COMPLEX; RECEPTOR; THIOUREA DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0242298259     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.09.207     Document Type: Article
Times cited : (67)

References (30)
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    • for recent reviews: (b) Lehn, J.-M. Angew. Chem., Int. Ed. Engl. 1988, 27, 89; (c) Schmidtchen, F. P.; Berger, M. Chem. Rev. 1997, 97, 1609; (d) Antonisse, M. M. G.; Reinhoudt, D. N. Chem. Commun. 1998, 443; (e) Gale, P. A. Coord. Chem. Rev. 2000, 199, 181; (f) Beer, P. D.; Gale, P. A. Angew. Chem., Int. Ed. 2001, 40, 486.
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    • Schmidtchen, F.P.1    Berger, M.2
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    • for recent reviews: (b) Lehn, J.-M. Angew. Chem., Int. Ed. Engl. 1988, 27, 89; (c) Schmidtchen, F. P.; Berger, M. Chem. Rev. 1997, 97, 1609; (d) Antonisse, M. M. G.; Reinhoudt, D. N. Chem. Commun. 1998, 443; (e) Gale, P. A. Coord. Chem. Rev. 2000, 199, 181; (f) Beer, P. D.; Gale, P. A. Angew. Chem., Int. Ed. 2001, 40, 486.
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    • for recent reviews: (b) Lehn, J.-M. Angew. Chem., Int. Ed. Engl. 1988, 27, 89; (c) Schmidtchen, F. P.; Berger, M. Chem. Rev. 1997, 97, 1609; (d) Antonisse, M. M. G.; Reinhoudt, D. N. Chem. Commun. 1998, 443; (e) Gale, P. A. Coord. Chem. Rev. 2000, 199, 181; (f) Beer, P. D.; Gale, P. A. Angew. Chem., Int. Ed. 2001, 40, 486.
    • (2000) Coord. Chem. Rev. , vol.199 , pp. 181
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    • for recent reviews: (b) Lehn, J.-M. Angew. Chem., Int. Ed. Engl. 1988, 27, 89; (c) Schmidtchen, F. P.; Berger, M. Chem. Rev. 1997, 97, 1609; (d) Antonisse, M. M. G.; Reinhoudt, D. N. Chem. Commun. 1998, 443; (e) Gale, P. A. Coord. Chem. Rev. 2000, 199, 181; (f) Beer, P. D.; Gale, P. A. Angew. Chem., Int. Ed. 2001, 40, 486.
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    • The skeleton of 2,2′-binaphthalene is found in natural products such as gossypol (1,1′,6,6′,7,7′-hexahydroxy-3,3′- dimethyl-5,5′-bis(1-methylethyl)[2,2′-binaphthalene]-8, 8′-dicarboxaldehyde) which is a natural toxin present in the cotton (Gossypium sp.) seed. See:
    • The skeleton of 2,2′-binaphthalene is found in natural products such as gossypol (1,1′,6,6′,7,7′-hexahydroxy-3,3′- dimethyl-5,5′-bis(1-methylethyl)[2,2′-binaphthalene]-8, 8′-dicarboxaldehyde) which is a natural toxin present in the cotton (Gossypium sp.) seed. See: Adams R., Geissman T.A., Edwards J.D. Chem. Rev. 60:1960;555.
    • (1960) Chem. Rev. , vol.60 , pp. 555
    • Adams, R.1    Geissman, T.A.2    Edwards, J.D.3
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    • note
    • +: m/z 513.2; found: 513.3.
  • 30
    • 85030942123 scopus 로고    scopus 로고
    • note
    • 2=0.150 (2796 reflections) and GOF=0.98 for 172 parameters. Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 217176. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.