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Volumn 38, Issue 6, 1990, Pages 1527-1535

Preparation of New Nitrogen-Bridged Heterocycles. XXII.1 a New Approach to the Syntheses of Thienoindolizine Derivatives

Author keywords

2 a indolizine thieno 2; 2 indolizinethiol thieno 3; 2 (substituted ethyl)thio indolizine; 2 (substituted methyl)thio indolizine; 3 fr indolizine alkylation; deprotection

Indexed keywords

INDOLIZINE DERIVATIVE;

EID: 0024992083     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.38.1527     Document Type: Article
Times cited : (21)

References (5)
  • 2
    • 0024544448 scopus 로고
    • A. Kakehi, S. Ito, T. Fujii, S. Matsumoto, Y. Morimoto, and M. Shiohara, Bull. Chem. Soc. Jpn., 62, 119 (1989).
    • A. Kakehi, S. Ito, S. Matsumoto, and Y. Morimoto, Chem. Lett., 1987, 2043; A. Kakehi, S. Ito, T. Fujii, S. Matsumoto, Y. Morimoto, and M. Shiohara, Bull. Chem. Soc. Jpn., 62, 119 (1989).
    • (1987) Chem. Lett. , pp. 2043
    • Kakehi, A.1    Ito, S.2    Matsumoto, S.3    Morimoto, Y.4
  • 3
    • 85008079579 scopus 로고    scopus 로고
    • Some of these thieno[2, 3-6\indolizine derivatives were recently found to show anti-HIV (human immuno deficiency virus) activity
    • Some of these thieno[2,3-6\indolizine derivatives were recently found to show anti-HIV (human immuno deficiency virus) activity.
  • 4
    • 85008083043 scopus 로고
    • Heterocycles
    • A. Kakehi, S. Ito, S. Yonezu, K. Maruta, K. Yuito, M. Shiohara and K. Adachi, Bull. Chem. Soc. Jpn., 60, 1867 (1987); A. Kakehi, S. Ito, N. Kinoshita, and Y. Abaka, Bull. Chem. Soc. Jpn., 61, 2055 (1988).
    • A. Kakehi, S. Ito, S. Yonezu, K. Maruta, and K. Yuito, Heterocycles, 23, 33 (1985); A. Kakehi, S. Ito, S. Yonezu, K. Maruta, K. Yuito, M. Shiohara and K. Adachi, Bull. Chem. Soc. Jpn., 60, 1867 (1987); A. Kakehi, S. Ito, N. Kinoshita, and Y. Abaka, Bull. Chem. Soc. Jpn., 61, 2055 (1988).
    • (1985) , vol.23 , Issue.33
    • Kakehi, A.1    Ito, S.2    Yonezu, S.3    Maruta, K.4    Yuito, K.5
  • 5
    • 85008083048 scopus 로고    scopus 로고
    • Although these unidentified compounds seem to be intermolecular condensation products of indolizines 4p, q from their elemental and spectral analyses, their structures are still uncertain
    • Although these unidentified compounds seem to be intermolecular condensation products of indolizines 4p, q from their elemental and spectral analyses, their structures are still uncertain.


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