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Volumn 6, Issue 7, 2015, Pages 4179-4183

Organocatalytic asymmetric chlorinative dearomatization of naphthols

Author keywords

[No Author keywords available]

Indexed keywords

FUNCTIONAL GROUPS;

EID: 84935877462     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c5sc00494b     Document Type: Article
Times cited : (102)

References (64)
  • 34
    • 84922803949 scopus 로고    scopus 로고
    • During the preparation of this manuscript, two examples of Lewis acid catalyzed asymmetric dearomatization of naphthols were reported, see
    • S.-G. Wang Q. Yin C.-X. Zhuo S.-L. You Angew. Chem., Int. Ed. 2015 54 647
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 647
    • Wang, S.-G.1    Yin, Q.2    Zhuo, C.-X.3    You, S.-L.4
  • 63
    • 84904471603 scopus 로고    scopus 로고
    • The dearomatized products of phenol derivatives could be observed by NMR study, but unstable to be isolated For examples of catalytic asymmetric chlorination of carbonyl compounds, see
    • M. Wilking C. G. Daniliuc U. Hennecke Synlett 2014 1701
    • (2014) Synlett , pp. 1701
    • Wilking, M.1    Daniliuc, C.G.2    Hennecke, U.3
  • 64
    • 84890084361 scopus 로고    scopus 로고
    • references therein N-Chlorosuccinimide was also tested as an electrophilic chlorination reagent, however, the reaction was slow and took several days for complete conversion The relative configurations of products 3c and 3d were determined by NOESY NMR analysis, see the ESI
    • K. Shibatomi A. Narayama Asian J. Org. Chem. 2013 2 812
    • (2013) Asian J. Org. Chem. , vol.2 , pp. 812
    • Shibatomi, K.1    Narayama, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.