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Volumn 130, Issue 12, 2009, Pages 1145-1150

A new strategy for the synthesis of fluorinated 3,4-dihydropyrimidinones

Author keywords

Fluorinated dihydropyrimidinones; Fluorinated nitriles; Intramolecular aza Michael reaction; Multicomponent reactions

Indexed keywords


EID: 70449530757     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2009.06.001     Document Type: Article
Times cited : (10)

References (33)
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    • 65249174168 scopus 로고    scopus 로고
    • For recent reviews of Biginelli and other multicomponent reactions, see: (a) S.V. Vdovina, V.A. Mamedov, Russ. Chem. Rev. 77 (2008), 1017-1053
    • (2008) Russ. Chem. Rev. , vol.77 , pp. 1017-1053
    • Vdovina, S.V.1    Mamedov, V.A.2
  • 18
    • 0003601534 scopus 로고
    • M. Windholz Ed, Merck and Co. Inc, Rahway
    • M. Windholz (Ed.), The Merck Index, Merck and Co. Inc., Rahway, 1976, p. 853.
    • (1976) The Merck Index , pp. 853
  • 21
    • 84995335222 scopus 로고    scopus 로고
    • D. Bozing, P. Benko, L. Petocz, M. Szecsey, P. Toempe, G. Gigler, I. Gacsalyi, Eur. Pat. Appl. EP (1991) 409, 233 [Chem. Abstr. 114 (1991) 247302z].
  • 31
    • 0000711429 scopus 로고    scopus 로고
    • For the preparation of gem-difluorinated nitriles 7, see: (a) Ref. [14]; (b) W.J. Middleton, E.M. Bingham, J. Org. Chem. 45 (1980) 2883-2887.
  • 32
    • 84995317242 scopus 로고    scopus 로고
    • The absolute configuration of the newly created stereocenter was not determined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.