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Volumn 52, Issue 3, 2013, Pages 866-869

The acetal concept: Regioselective access to ortho,ortho-diphenols via dibenzo-1,3-dioxepines

Author keywords

acetal tethers; biphenols; dioxepines; diphenols; radical cyclization

Indexed keywords

BIPHENOLS; CHIRAL LIGAND; DIOXEPINES; DIPHENOLS; HYDROLYTIC CLEAVAGE; NATURAL PRODUCTS; RADICAL CYCLIZATIONS; REGIO-SELECTIVE; STRUCTURAL MOTIFS;

EID: 84872281971     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201207485     Document Type: Article
Times cited : (45)

References (49)
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    • (2004) Metal-Catalyzed Cross-Coupling Reactions
    • Bräse, S.1    Meijere, A.D.2
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    • PRPR 45.
    • J. M. Brunel, Chem. Rev. 2007, 107, PR 1 -PR 45.
    • (2007) Chem. Rev. , vol.107 , pp. 1
    • Brunel, J.M.1
  • 29
    • 0002101765 scopus 로고
    • The one literature claim of satisfactory dimerization of 1-naphthol is erroneous; inspection of the spectra clearly indicates that the material re-isolated is the monomer (i.e. substrate)
    • Y. Kashiwagi, H. Ono, T. Osa, Chem. Lett. 1993, 81. The one literature claim of satisfactory dimerization of 1-naphthol is erroneous; inspection of the spectra clearly indicates that the material re-isolated is the monomer (i.e. substrate)
    • (1993) Chem. Lett. , pp. 81
    • Kashiwagi, Y.1    Ono, H.2    Osa, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.