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Volumn 38, Issue 38, 1997, Pages 6697-6700

Synthesis and absolute configuration of (-)-normalindine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID;

EID: 0030880842     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01568-2     Document Type: Article
Times cited : (31)

References (31)
  • 1
    • 0023554289 scopus 로고
    • For isolation of some alkaloids containing this ring system, see (a) and references cited therein;
    • For isolation of some alkaloids containing this ring system, see (a) Jahangir; Brook, M.A.; MacLean, D. B.; Holland, H.L. Tetrahedron 1987, 43, 5761-5768 and references cited therein;
    • (1987) Tetrahedron , vol.43 , pp. 5761-5768
    • Jahangir Brook, M.A.1    MacLean, D.B.2    Holland, H.L.3
  • 8
    • 0000268153 scopus 로고
    • For a recent review on the Diels-Alder reaction of oxazoles, see
    • For a recent review on the Diels-Alder reaction of oxazoles, see Hassner, A.; Fischer, B. Heterocycles 1993, 35, 1441-1465.
    • (1993) Heterocycles , vol.35 , pp. 1441-1465
    • Hassner, A.1    Fischer, B.2
  • 9
    • 0020563556 scopus 로고
    • Several examples of intramolecular oxazole-olefin Diels-Alder reactions have been reported: (a)
    • Several examples of intramolecular oxazole-olefin Diels-Alder reactions have been reported: (a) Levin, J. I.; Weinreb, S.M. J. Am. Chem. Soc. 1983, 105, 1397-1398;
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 1397-1398
    • Levin, J.I.1    Weinreb, S.M.2
  • 16
    • 0343599021 scopus 로고    scopus 로고
    • Satisfactory analytical and/or spectroscopic data were obtained for all new compounds described
    • Satisfactory analytical and/or spectroscopic data were obtained for all new compounds described.
  • 22
    • 33748542524 scopus 로고
    • For earlier reviews, see (a)
    • For earlier reviews, see (a) Johnson, F. Chem. Rev. 1968, 68, 375-413;
    • (1968) Chem. Rev. , vol.68 , pp. 375-413
    • Johnson, F.1
  • 24
    • 0343599019 scopus 로고    scopus 로고
    • 3), which is explicable by assuming the presence of intramolecular hydrogen bonding between the NH and ester carbonyl groups
    • 3), which is explicable by assuming the presence of intramolecular hydrogen bonding between the NH and ester carbonyl groups.
  • 27
    • 84942695755 scopus 로고
    • (a)
    • (a) Bohlmann, F. Chem. Ber. 1958, 91, 2157-2167;
    • (1958) Chem. Ber. , vol.91 , pp. 2157-2167
    • Bohlmann, F.1
  • 29
    • 0343599018 scopus 로고    scopus 로고
    • Treatment of 18 with AcOH under similar conditions resulted in the contraction of ring D accompanied by dehydration. The details will be reported elsewhere
    • Treatment of 18 with AcOH under similar conditions resulted in the contraction of ring D accompanied by dehydration. The details will be reported elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.