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Volumn 46, Issue 46, 2007, Pages 8854-8857

Spirofungin A: Stereoselective synthesis and inhibition of isoleucyl-tRNA synthetase

Author keywords

Metathesis; Natural products; Spiroketals; Stereocontrolled synthesis; tRNA synthetase

Indexed keywords

CHEMICAL EQUATIONS; METATHESIS; POLYKETIDES; SPIROKETALS; STEREOCONTROLLED SYNTHESIS;

EID: 36749093348     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702440     Document Type: Article
Times cited : (47)

References (26)
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    • For a diastereoselective approach to spiroketal subunit of spirofungin B, see
    • For a diastereoselective approach to spiroketal subunit of spirofungin B, see T. E. La Cruz, S. D. Rychnovsky, Org. Lett. 2005, 7, 1873-1876.
    • (2005) Org. Lett , vol.7 , pp. 1873-1876
    • La Cruz, T.E.1    Rychnovsky, S.D.2
  • 12
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    • A nearly equimolar mixture of spiroketals 2 and 3 is typically obtained upon spontaneous spiroketalization (see Refs. [7] and [8]).
    • A nearly equimolar mixture of spiroketals 2 and 3 is typically obtained upon spontaneous spiroketalization (see Refs. [7] and [8]).
  • 13
    • 0032510338 scopus 로고    scopus 로고
    • For a review of disposable tethers, see
    • For a review of disposable tethers, see D. R. Gauthier, K. S. Zandi, K. J. Shea, Tetrahedron 1998, 54, 2289-2338.
    • (1998) Tetrahedron , vol.54 , pp. 2289-2338
    • Gauthier, D.R.1    Zandi, K.S.2    Shea, K.J.3
  • 14
    • 0346366645 scopus 로고    scopus 로고
    • For the use of a cyclic sulfide to control spiroketalization, see
    • For the use of a cyclic sulfide to control spiroketalization, see Y. Ishikawa, S. Nishiyama, Tetrahedron Lett. 2004, 45, 351-354.
    • (2004) Tetrahedron Lett , vol.45 , pp. 351-354
    • Ishikawa, Y.1    Nishiyama, S.2
  • 18
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    • For details, see the Supporting Information
    • For details, see the Supporting Information.
  • 20
    • 0037078848 scopus 로고    scopus 로고
    • For ring-closing metathesis using temporary silicon tethers, see a
    • For ring-closing metathesis using temporary silicon tethers, see a) P. Van de Weghe, D. Aoun, J.-G. Boiteau, J. Eustache, Org. Lett. 2002, 4, 4105-4108;
    • (2002) Org. Lett , vol.4 , pp. 4105-4108
    • Van de Weghe, P.1    Aoun, D.2    Boiteau, J.-G.3    Eustache, J.4
  • 22
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    • ORTEP representation of tricyclic silane 26 prepared during our initial studies of spiroketalization; for details, see the Supporting Information. CCDC-658800 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. (Chemical Equation Presented)
    • ORTEP representation of tricyclic silane 26 prepared during our initial studies of spiroketalization; for details, see the Supporting Information. CCDC-658800 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. (Chemical Equation Presented)
  • 25
    • 4043088534 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 2259-2263.
    • (2004) Chem. Int. Ed , vol.43 , pp. 2259-2263
    • Angew1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.