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Volumn 49, Issue 49, 2008, Pages 7018-7020

Corrigendum to "A chemoenzymatic synthesis of the anti-influenza agent Tamiflu®" [Tetrahedron Lett. 49 (2008) 7018] (DOI:10.1016/j.tetlet.2008.09.130);A chemoenzymatic synthesis of the anti-influenza agent Tamiflu®

Author keywords

Acylaziridine; Anti influenza; cis 1,2 Dihydrocatechol; Synthesis; Tamiflu

Indexed keywords

BROMOBENZENE; CATECHOL DERIVATIVE; CIS 1,2 DIHYDROCATECHOL; OSELTAMIVIR; UNCLASSIFIED DRUG;

EID: 54049095827     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.04.015     Document Type: Erratum
Times cited : (64)

References (34)
  • 3
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    • and references therein
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    • McClellan, K.1    Perry, C.M.2
  • 5
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    • Fuyuno, I.1
  • 8
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    • See, for example: http://www.roche.com/med-cor-2006-04-19.
    • See, for example: http://www.roche.com/med-cor-2006-04-19.
  • 11
    • 46849088854 scopus 로고    scopus 로고
    • For a recent survey of activities in this area see: and references therein
    • For a recent survey of activities in this area see:. Shibasaki M., and Kanai M. Eur. J. Org. Chem. (2008) 1839 and references therein
    • (2008) Eur. J. Org. Chem. , pp. 1839
    • Shibasaki, M.1    Kanai, M.2
  • 26
    • 0001846314 scopus 로고    scopus 로고
    • Compound 2 can be obtained from the Aldrich Chemical Co. (Catalogue Number 489492) or from Questor, Queen's University of Belfast, Northern Ireland (see: http://questor.qub.ac.uk/newsite/contact.htm). For reviews on methods for generating cis-1,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as on the synthetic applications of these metabolites, see:
    • Compound 2 can be obtained from the Aldrich Chemical Co. (Catalogue Number 489492) or from Questor, Queen's University of Belfast, Northern Ireland (see: http://questor.qub.ac.uk/newsite/contact.htm). For reviews on methods for generating cis-1,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as on the synthetic applications of these metabolites, see:. Hudlicky T., Gonzalez D., and Gibson D.T. Aldrichim. Acta 32 (1999) 35
    • (1999) Aldrichim. Acta , vol.32 , pp. 35
    • Hudlicky, T.1    Gonzalez, D.2    Gibson, D.T.3
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    • note
    • 6 proved to be the most effective.
  • 32
    • 54049131805 scopus 로고    scopus 로고
    • note
    • Selected physical and spectral data for compound 11 are presented in the Supplementary data.
  • 33
    • 54049100836 scopus 로고    scopus 로고
    • note
    • max = 55°); R = 0.025 [for 2899 with I > 2.0σ(I)]; Rw = 0.044 (all data), S = 0.99. Images were measured on a Nonius Kappa CCD diffractometer (MoKα, graphite monochromator, λ = 0.71073 Å). Crystallographic data for compound 11 have been deposited with the Cambridge Crystallographic Data Center (CCDC no. 701227). These data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (email: data_request@ccdc.cam.ac.uk, fax: +44 1223 336033, or via http://www.ccdc.cam.ac.uk/data_request/cif).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.