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Volumn , Issue 11, 1999, Pages 3151-3153

vic-difluorination of fluoroalkenes with xenon difiuoride: The effect of fluorine substituents on the reaction of alkenes with xenon difluoride

Author keywords

Alkenes; Fluorine; Fluoroalkenes; Vic Difluorination; Xenon difluoride

Indexed keywords

ALKENE; CATION; FLUORIDE; UNCLASSIFIED DRUG; XENON; XENON DIFLUORIDE;

EID: 0032698823     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199911)1999:11<3151::aid-ejoc3151>3.0.co;2-f     Document Type: Article
Times cited : (6)

References (20)
  • 2
    • 0028361921 scopus 로고
    • For example, see A. Toyota, J. Chiba, Y. Sugita, M. Sato, C. Kaneko, Chem. Pharm. Bull. 1994, 42, 459-461; M. Sato, T. Hirokawa, H. Hattori, A. Toyota, C. Kaneko, Tetrahedron: Asymmetry 1994, 5, 975-980; A. Toyota, M. Aizawa, C. Habutani, N. Katagiri, C. Kaneko, Tetrahedron 1995, 51, 8783-8797.
    • (1994) Chem. Pharm. Bull. , vol.42 , pp. 459-461
    • Toyota, A.1    Chiba, J.2    Sugita, Y.3    Sato, M.4    Kaneko, C.5
  • 3
    • 0028246439 scopus 로고
    • For example, see A. Toyota, J. Chiba, Y. Sugita, M. Sato, C. Kaneko, Chem. Pharm. Bull. 1994, 42, 459-461; M. Sato, T. Hirokawa, H. Hattori, A. Toyota, C. Kaneko, Tetrahedron: Asymmetry 1994, 5, 975-980; A. Toyota, M. Aizawa, C. Habutani, N. Katagiri, C. Kaneko, Tetrahedron 1995, 51, 8783-8797.
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 975-980
    • Sato, M.1    Hirokawa, T.2    Hattori, H.3    Toyota, A.4    Kaneko, C.5
  • 4
    • 0029123806 scopus 로고
    • For example, see A. Toyota, J. Chiba, Y. Sugita, M. Sato, C. Kaneko, Chem. Pharm. Bull. 1994, 42, 459-461; M. Sato, T. Hirokawa, H. Hattori, A. Toyota, C. Kaneko, Tetrahedron: Asymmetry 1994, 5, 975-980; A. Toyota, M. Aizawa, C. Habutani, N. Katagiri, C. Kaneko, Tetrahedron 1995, 51, 8783-8797.
    • (1995) Tetrahedron , vol.51 , pp. 8783-8797
    • Toyota, A.1    Aizawa, M.2    Habutani, C.3    Katagiri, N.4    Kaneko, C.5
  • 8
  • 10
    • 0344355046 scopus 로고    scopus 로고
    • note
    • vic-Difluorination of aliphatic alkenes using xenon difluoride has been reported in the case of very specific substrates.[7,15-17]
  • 16
    • 0004098366 scopus 로고
    • John Wiley & Sons Inc., ch. 1
    • R. D. Chambers, Fluorine in Organic Chemistry; John Wiley & Sons Inc., 1973, ch. 1; G. A. Olah, Y. K. Mo, Adv. Fluorine Chem. 1973, 7, 69-112.
    • (1973) Fluorine in Organic Chemistry
    • Chambers, R.D.1
  • 17
    • 0042663797 scopus 로고
    • R. D. Chambers, Fluorine in Organic Chemistry; John Wiley & Sons Inc., 1973, ch. 1; G. A. Olah, Y. K. Mo, Adv. Fluorine Chem. 1973, 7, 69-112.
    • (1973) Adv. Fluorine Chem. , vol.7 , pp. 69-112
    • Olah, G.A.1    Mo, Y.K.2
  • 18
    • 0345649605 scopus 로고    scopus 로고
    • note
    • 4 afforded the corresponding product in 90% yield although the substrate is an alkyl-substituted fluoroalkene.[16] However, this result would appear to be very specific and seems to depend on the substrate - vic-difluorination of 1-fluorocyohexene under the same reaction conditions resulted in less than 30% yield according to our experiment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.