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Volumn 14, Issue 11, 2012, Pages 2682-2685

A formal synthesis of (-)-englerin A by relay ring closing metathesis and transannular etherification

Author keywords

[No Author keywords available]

Indexed keywords

ENGLERIN A; SESQUITERPENE;

EID: 84861796587     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol3007524     Document Type: Article
Times cited : (48)

References (31)
  • 18
    • 1542759075 scopus 로고
    • See, however, the regiospecific ring opening of vinyl substituted examples
    • See, however, the regiospecific ring opening of vinyl substituted examples: Narjes, F.; Schaumann, E. Liebigs Ann. Chem 1993, 841
    • (1993) Liebigs Ann. Chem , pp. 841
    • Narjes, F.1    Schaumann, E.2
  • 19
    • 0001025010 scopus 로고
    • In addition, one might note the successful addition of acetylide to the 3-position of 2-substituted 2,3-epoxy esters
    • In addition, one might note the successful addition of acetylide to the 3-position of 2-substituted 2,3-epoxy esters: Bartlett, P. A.; Tanzella, D. J.; Barstow, J. F. J. Org. Chem. 1982, 47, 3941
    • (1982) J. Org. Chem. , vol.47 , pp. 3941
    • Bartlett, P.A.1    Tanzella, D.J.2    Barstow, J.F.3
  • 24
    • 37049137254 scopus 로고
    • The known bromide 12 was prepared from the corresponding alcohol (see the Supporting Information) by the method of
    • The known bromide 12 was prepared from the corresponding alcohol (see the Supporting Information) by the method of Barton, D. H.; Shioiri, T.; Widdowson, D. A. J. Chem. Soc. C 1971, 1968
    • (1971) J. Chem. Soc. C , pp. 1968
    • Barton, D.H.1    Shioiri, T.2    Widdowson, D.A.3
  • 26
    • 78249268215 scopus 로고    scopus 로고
    • This result may be compared with the nonspecific, nonrelay ene-yne-ene metathesis of a similar, highly substituted system in which reaction, carried out under ethylene, is presumably initiated at the acetylene; see
    • This result may be compared with the nonspecific, nonrelay ene-yne-ene metathesis of a similar, highly substituted system in which reaction, carried out under ethylene, is presumably initiated at the acetylene; see: Knueppel, S.; Rogachev, V. O.; Metz, P. Eur. J. Org. Chem. 2010, 6145
    • (2010) Eur. J. Org. Chem. , pp. 6145
    • Knueppel, S.1    Rogachev, V.O.2    Metz, P.3
  • 29
    • 37049102895 scopus 로고
    • One should note that this result is not inconsistent with regiochemistry observed in the oxymercuration of simple conjugated dienes; see
    • One should note that this result is not inconsistent with regiochemistry observed in the oxymercuration of simple conjugated dienes; see: Barluenga, J.; Perez-Prieto, J.; Asensio, G. J. Chem. Soc., Perkin Trans. 1 1984, 629
    • (1984) Chem. Soc., Perkin Trans. 1 , pp. 629
    • Barluenga, J.1    Perez-Prieto, J.2    Asensio, G.J.3
  • 31
    • 77952397509 scopus 로고    scopus 로고
    • This alcohol is a known compound, prepared from alcohol 17 in two steps and 60% yield as described in
    • This alcohol is a known compound, prepared from alcohol 17 in two steps and 60% yield as described in Molawi, K.; Delpont, N; Echavarren, A. M. Angew. Chem., Int. Ed. 2010, 49, 3517
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 3517
    • Molawi, K.1    Delpont, N.2    Echavarren, A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.