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Volumn 47, Issue 20, 2008, Pages 3787-3790

A chiral hypervalent iodine(III) reagent for enantioselective dearomatization of phenols

Author keywords

Asymmetric synthesis; Hypervalent compounds; Iodine; Oxidation; Quinones

Indexed keywords

CHEMICAL REACTIONS; INDUSTRIAL CHEMICALS; IODINE;

EID: 45549094716     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800464     Document Type: Article
Times cited : (437)

References (61)
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  • 37
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    • Selected works for stereoselective dearomatization of phenols: a L. H. Mejorado, C. Hoarau, T. R. R. Pettus, Org. Lett. 2004, 6, 1535;
    • Selected works for stereoselective dearomatization of phenols: a) L. H. Mejorado, C. Hoarau, T. R. R. Pettus, Org. Lett. 2004, 6, 1535;
  • 41
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    • Recent reports of natural product syntheses containing chiral ortho-spirolactone structures: a T. Siu, C. D. Cox, S. J. Danishefsky, Angew. Chem. 2003, 115, 5787;
    • Recent reports of natural product syntheses containing chiral ortho-spirolactone structures: a) T. Siu, C. D. Cox, S. J. Danishefsky, Angew. Chem. 2003, 115, 5787;
  • 44
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    • In contrast, the cyclohexa-2,4-dienones obtained from the oxidation of phenols are generally quite reactive and are useful for subsequent transformations. See, references [3] and [4].
    • In contrast, the cyclohexa-2,4-dienones obtained from the oxidation of phenols are generally quite reactive and are useful for subsequent transformations. See, references [3] and [4].
  • 45
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    • The 1,1′-spirobiindane backbone has been introduced as an elegant ligand for transition metals in asymmetric syntheses: a V. B. Birman, A. L. Rheingold, K. C. Lam, Tetrahedron: Asymmetry 1999, 10, 125;
    • The 1,1′-spirobiindane backbone has been introduced as an elegant ligand for transition metals in asymmetric syntheses: a) V. B. Birman, A. L. Rheingold, K. C. Lam, Tetrahedron: Asymmetry 1999, 10, 125;
  • 50
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    • Although (R)-9 could be obtained by using mCPBA in AcOH/CH2Cl2, higher purity of (R)-9 was obtained by the method using Selectfluor
    • 2, higher purity of (R)-9 was obtained by the method using Selectfluor.
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    • T. Dohi, A. Maruyama, Y. Minamitsuji, N . Takenaga, Y. Kita, Chem. Commun. 2007, 1189.
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    • Reviews: a
    • Reviews: a) T. Dohi, Y. Kita, Kagaku 2006, 61, 68;
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    • Dohi, T.1    Kita, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.