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Volumn 52, Issue 51, 2011, Pages 6887-6889

Protecting group free syntheses of (±)-columbianetin and (±)-angelmarin

Author keywords

Angelmarin; Aromatization; Columbianetin; Coumarin; Intramolecular hydroarylation

Indexed keywords

ARTICLE; ENANTIOSELECTIVITY;

EID: 81255129274     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.10.036     Document Type: Article
Times cited : (22)

References (19)
  • 14
    • 0028897466 scopus 로고
    • Compound 8 is an established precursor to the angular furanocoumarin oroselol. See: Y.R. Lee Tetrahedron 51 1995 3087
    • (1995) Tetrahedron , vol.51 , pp. 3087
    • Lee, Y.R.1
  • 15
    • 0014708757 scopus 로고
    • Compound (±)-9 has been prepared previously, in nine steps from 2,6-dihydroxybenzoic acid, and used in a synthesis of (±)-columbianetin. See: M. Shipchandler, T.O. Soine, and P.K. Gupta J. Pharm. Sci. 59 1970 67
    • (1970) J. Pharm. Sci. , vol.59 , pp. 67
    • Shipchandler, M.1    Soine, T.O.2    Gupta, P.K.3
  • 19
    • 0001373492 scopus 로고
    • The R-enantiomeric form of the iodo-analog of compound (±)-12 has been prepared using Sharpless asymmetric epoxidation techniques: X.-y. Xiao, S.-K. Park, and G.D. Prestwich J. Org. Chem. 53 1988 4869
    • (1988) J. Org. Chem. , vol.53 , pp. 4869
    • Xiao, X.-Y.1    Park, S.-K.2    Prestwich, G.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.