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Volumn 26, Issue 20, 1985, Pages 2459-2462

New synthetic methods for 4-amino-2(5H)-furanones

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Indexed keywords


EID: 0001530076     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)94853-6     Document Type: Article
Times cited : (21)

References (14)
  • 1
    • 84918389839 scopus 로고    scopus 로고
    • P.E. Aldrich, Japan Tokkyo Kokai Koho 77-139056; Chem. Abstr., 88, 169947s.
  • 2
    • 84918389838 scopus 로고    scopus 로고
    • B.I. Dittmar and W.A. Price, Jr., Ger. Patent 2516555; Japan Tokkyo Kokai Koho 75-148352; Chem. Abstr., 84, 74087q.
  • 3
    • 84918389837 scopus 로고    scopus 로고
    • 2
  • 12
    • 0000631744 scopus 로고
    • Studies on the intramolecular Claisen condensation: facile synthesis of tetronic acids
    • 2, Similar base promoted transformation of α-acetoxyalkanoic esters to tetronic acids is reported.
    • (1984) The Journal of Organic Chemistry , vol.49 , pp. 927
    • Brandäge1    Flodman2    Norberg3
  • 14
    • 84918389836 scopus 로고    scopus 로고
    • When 4b was treated with dil hydrochloric acid (3% aq HCl-EtOH 1 : 3, r.t., 20 min), hydrolysis of the O-protecting group and the enamine moiety took place to give t-butyl 4-hydroxy-3-oxo-pentanoate in a quantitative yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.