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Volumn 53, Issue 29, 2012, Pages 3746-3749

Reactivity of the ester group attached isoxazoline, benzisoxazole, and isoxazole: A facial preparation of 3-acyl-substituted these heterocycles

Author keywords

Benzisoxazoles; Heterocyclic chemistry; Isoxazoles; Isoxazolines; Ketone

Indexed keywords

ALKYNYL GROUP; BENZISOXAZOLE; ESTER; GRIGNARD REAGENT; HETEROCYCLIC COMPOUND; ISOXAZOLE; ISOXAZOLE DERIVATIVE; ISOXAZOLINE DERIVATIVE; LITHIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84862201298     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.05.006     Document Type: Article
Times cited : (8)

References (47)
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    • Nahm, S.1    Weinreb, S.M.2
  • 32
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    • For examples of the reports on synthesis of 3-methyl keto and aryl keto isoxazolines and benzisoxazolines, see: T. Jen, B.A. Mendelsohn, and M.A. Ciufolini J. Org. Chem. 76 2011 728 731
    • (2011) J. Org. Chem. , vol.76 , pp. 728-731
    • Jen, T.1    Mendelsohn, B.A.2    Ciufolini, M.A.3
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    • 0037294679 scopus 로고    scopus 로고
    • Among heterocyclic compounds, only 4-methoxycarbonyloxazolidinone is employed to introduction of alkynyl groups, see
    • Among heterocyclic compounds, only 4-methoxycarbonyloxazolidinone is employed to introduction of alkynyl groups, see: T. Hakogi, T. Shigenari, S. Katsumura, T. Sano, T. Kohno, and Y. Igarashi Bioorg. Med. Chem. Lett. 13 2003 661 664
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 661-664
    • Hakogi, T.1    Shigenari, T.2    Katsumura, S.3    Sano, T.4    Kohno, T.5    Igarashi, Y.6
  • 46
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    • For examples of synthesis and biological activity of benzisoxazoline containing bis-heterocyclic compounds, see
    • For examples of synthesis and biological activity of benzisoxazoline containing bis-heterocyclic compounds, see: G.M. Shutske, L.L. Setescak, R.C. Allen, L. Davis, R.C. Effland, and K.J. Ranbom Med. Chem. 25 1982 36 44
    • (1982) Med. Chem. , vol.25 , pp. 36-44
    • Shutske, G.M.1    Setescak, L.L.2    Allen, R.C.3    Davis, L.4    Effland, R.C.5    Ranbom, K.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.