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Volumn 69, Issue 46, 2013, Pages 9609-9615

Formal meta-specific intramolecular Friedel-Crafts allylic alkylation of phenols through a spirocyclization-dienone-phenol rearrangement cascade

Author keywords

Alkylation; Cascade reaction; Friedel Crafts reaction; Rearrangement; Spiro compounds

Indexed keywords

ALKADIENE; DIENONE; PALLADIUM; PHENOL; PHENOL DERIVATIVE; SCANDIUM; UNCLASSIFIED DRUG;

EID: 84885174319     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.09.042     Document Type: Article
Times cited : (15)

References (45)
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    • For a review, see: V. Snieckus Chem. Rev. 90 1990 879 933
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    • Snieckus, V.1
  • 23
    • 0000185077 scopus 로고
    • For recent examples of dienone-phenol rearrangement of spirocyclohexadienones or spiro-type intermediates, see
    • B. Miller Acc. Chem. Res. 8 1975 245 256 For recent examples of dienone-phenol rearrangement of spirocyclohexadienones or spiro-type intermediates, see
    • (1975) Acc. Chem. Res. , vol.8 , pp. 245-256
    • Miller, B.1
  • 35
    • 79955488982 scopus 로고    scopus 로고
    • Compound 1a can be synthesized in high yield with excellent enantiomeric excess (97% ee) using the chiral Ir catalyst system developed by You, et al. See
    • Compound 1a can be synthesized in high yield with excellent enantiomeric excess (97% ee) using the chiral Ir catalyst system developed by You, et al. See: Q.-F. Wu, W.-B. Liu, C.-X. Zhuo, Z.-Q. Rong, K.-Y. Ye, and S.-L. You Angew. Chem., Int. Ed. 50 2011 4455 4458
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 4455-4458
    • Wu, Q.-F.1    Liu, W.-B.2    Zhuo, C.-X.3    Rong, Z.-Q.4    Ye, K.-Y.5    You, S.-L.6
  • 36
    • 33646775336 scopus 로고    scopus 로고
    • Our preceding paper relating to the one-pot sequential multi-catalytic process, see
    • Our preceding paper relating to the one-pot sequential multi-catalytic process, see: T. Nemoto, T. Fukuda, and Y. Hamada Tetrahedron Lett. 47 2006 4365 4368
    • (2006) Tetrahedron Lett. , vol.47 , pp. 4365-4368
    • Nemoto, T.1    Fukuda, T.2    Hamada, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.