메뉴 건너뛰기




Volumn , Issue 23, 2001, Pages 4501-4507

Synthesis of a fluorinated ether lipid analogous to a platelet activating factor

Author keywords

Allylic ether; Antitumoragents; Bromofluorination; Fluorine; Lipase catalyzed deracemization; Lipids

Indexed keywords

1 ACETOXY 2 FLUORO 3 HEXADECYLOXY 2 METHYLPROPANE; 2 FLUORO 3 HEXADECYLOXY 2 METHYLPROP 1 YL 2' (TRIMETHYLAMMONIO)ETHYL PHOSPHATE; 2 FLUORO 3 HEXADECYLOXY 2 METHYLPROPAN 1 OL; ALLYL COMPOUND; ANTINEOPLASTIC AGENT; CISPLATIN; ETHER LIPID; FLUORINE DERIVATIVE; ILMOFOSINE; THROMBOCYTE ACTIVATING FACTOR DERIVATIVE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

EID: 0035208386     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200112)2001:23<4501::AID-EJOC4501>3.0.CO;2-J     Document Type: Article
Times cited : (13)

References (76)
  • 25
    • 0003314351 scopus 로고    scopus 로고
    • Biomedical Frontiers of Fluorine Chemistry
    • American Chemical Society, Washington
    • [17c] Biomedical Frontiers of Fluorine Chemistry (Eds.: I. Ojima, J. R. McCarthy, J. T. Welch), ACS Symposium Series 639, American Chemical Society, Washington, 1996.
    • (1996) ACS Symposium Series 639
    • Ojima, I.1    McCarthy, J.R.2    Welch, J.T.3
  • 28
    • 0002780706 scopus 로고    scopus 로고
    • Asymmetric Fluoroorganic Chemistry, Synthesis, Applications, and Future Directions
    • American Chemical Society, Washington
    • [17f] Asymmetric Fluoroorganic Chemistry, Synthesis, Applications, and Future Directions (Ed.: P. V. Ramachandran), ACS Symposium Series 746, American Chemical Society, Washington, 2000.
    • (2000) ACS Symposium Series 746
    • Ramachandran, P.V.1
  • 35
    • 0000456403 scopus 로고    scopus 로고
    • Coordination Ability of Fluorine to Proton or Metals Based on Experimental and Theoretical Evidence
    • (Ed.: V. A. Soloshonok), John Wiley & Sons, Chichester
    • [19d] T. Yamazaki, T. Kitazume, Coordination Ability of Fluorine to Proton or Metals Based on Experimental and Theoretical Evidence, in: Enantiocontrolled Synthesis of Fluoro-Organic Compounds (Ed.: V. A. Soloshonok), John Wiley & Sons, Chichester, 1999, pp. 575-600.
    • (1999) Enantiocontrolled Synthesis of Fluoro-Organic Compounds , pp. 575-600
    • Yamazaki, T.1    Kitazume, T.2
  • 38
    • 0023237559 scopus 로고
    • [22a] J. T. Welch, Tetrahedron 1987, 43, 3123-3197.
    • (1987) Tetrahedron , vol.43 , pp. 3123-3197
    • Welch, J.T.1
  • 41
  • 47
    • 0006955623 scopus 로고    scopus 로고
    • note
    • 3N·3HF.
  • 51
    • 0006910295 scopus 로고    scopus 로고
    • note
    • Nucleophilic substitution of a bromine atom with an acetate function (step iii in Scheme 4) was significantly slower with vicinal bromofluoroalkanes than with the non-fluorinated parent compounds. As well as the modification of the electron density at the reaction center, electrostatic repulsion between the fluorine substituent and the approaching nucleophile seem to be important.
  • 64
    • 0006946783 scopus 로고    scopus 로고
    • PhD Thesis, University of Münster
    • A. Burchardt, PhD Thesis, University of Münster, 1999.
    • (1999)
    • Burchardt, A.1
  • 65
    • 33748448195 scopus 로고
    • 19F NMR). Esterification of the acid with (-)-menthol and DCC/DMAP according to the method described by A. Hassner, V. Alexanian, Tetrahedron Lett. 1978, 4475-4476,
    • (1978) Tetrahedron Lett. , pp. 4475-4476
    • Hassner, A.1    Alexanian, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.