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Volumn 3, Issue 15, 2001, Pages 2261-2264

Template-directed C-H insertion: Synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids

Author keywords

[No Author keywords available]

Indexed keywords

FUSED HETEROCYCLIC RINGS; OCTANE; TRICARBOXYLIC ACID;

EID: 0035954896     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0158361     Document Type: Article
Times cited : (34)

References (26)
  • 3
    • 0001331380 scopus 로고
    • Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Georg Thieme Verlag: Stuttgart
    • Taber, D. F. Methods of Organic Chemistry (Houben-Weyl); Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Georg Thieme Verlag: Stuttgart, 1995; Vol. E21a, pp 1127-1148.
    • (1995) Methods of Organic Chemistry (Houben-Weyl) , vol.E21A , pp. 1127-1148
    • Taber, D.F.1
  • 10
    • 0032537671 scopus 로고    scopus 로고
    • While this work was in progress, Wills and co-workers reported a related approach to the zaragozic acids based on alkylidene carbene insertion: Walker, L. F.; Connolly, S.; Wills, M. Tetrahedron Lett. 1998, 39, 5273-5276.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5273-5276
    • Walker, L.F.1    Connolly, S.2    Wills, M.3
  • 12
    • 0000505762 scopus 로고
    • 2-Carboxy-1,3-dioxanes display a pronounced preference (∼4 kcal/ mol) for the axially oriented 2-carboxylate group: Bailey, W. F.; Eliel, E. L. J. Am. Chem. Soc. 1974, 96, 1798-1806.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 1798-1806
    • Bailey, W.F.1    Eliel, E.L.2
  • 23
    • 0000418813 scopus 로고
    • Axially orientated 2-methoxy-1,3-dioxanes are known to undergo nucleophilic substitution with retention at C-2: (a) Eliel, E. L.; Nader, F. W. J. Am. Chem. Soc. 1970, 92, 584-590.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 584-590
    • Eliel, E.L.1    Nader, F.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.