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Volumn 75, Issue 21, 2010, Pages 7393-7399

Polyfluorination using IF5

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC RINGS; ARYLATIONS; CARBONYL COMPOUNDS; CARBONYL GROUPS; FLUORINE ATOMS; FRIEDEL-CRAFTS;

EID: 78049514481     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101672g     Document Type: Article
Times cited : (15)

References (29)
  • 9
    • 33747237825 scopus 로고    scopus 로고
    • In, Blackwell Publishing: Oxford,; Chapter 7, p
    • Uneyama, K. In Organofluorine Chemistry, Blackwell Publishing: Oxford, 2006; Chapter 7, p 223.
    • (2006) Organofluorine Chemistry , pp. 223
    • Uneyama, K.1
  • 21
    • 0007062675 scopus 로고
    • For the Friedel-Crafts-type alkylation of aromatic compounds using alkyl fluorides, see
    • For the Friedel-Crafts-type alkylation of aromatic compounds using alkyl fluorides, see: Olah, G. A.; Farooq, O.; Farnia, S. M. F.; Wu, A. J. Org. Chem. 1990, 55, 1516
    • (1990) J. Org. Chem. , vol.55 , pp. 1516
    • Olah, G.A.1    Farooq, O.2    Farnia, S.M.F.3    Wu, A.4
  • 22
    • 63049139266 scopus 로고    scopus 로고
    • For the Friedel-Crafts-type alkylation using α-halosulfides, see:; Chem. Pharm. Bull. 1982, 30, 915
    • Aoyama, M.; Hara, S. Tetrahedron 2009, 65, 3682 For the Friedel-Crafts-type alkylation using α-halosulfides, see: Tamura, Y.; Choi, H. D.; Shindo, H.; Ishibashi, H. Chem. Pharm. Bull. 1982, 30, 915
    • (2009) Tetrahedron , vol.65 , pp. 3682
    • Aoyama, M.1    Hara, S.2    Tamura, Y.3    Choi, H.D.4    Shindo, H.5    Ishibashi, H.6
  • 26
    • 0036328374 scopus 로고    scopus 로고
    • 3N-3HF was used for the oxidative fluorination reaction of the sulfides; see
    • 3N-3HF was used for the oxidative fluorination reaction of the sulfides; see: Ayuba, S.; Yoneda, N.; Fukuhara, T.; Hara, S. Bull. Chem. Soc. Jpn. 2002, 75, 1597
    • (2002) Bull. Chem. Soc. Jpn. , vol.75 , pp. 1597
    • Ayuba, S.1    Yoneda, N.2    Fukuhara, T.3    Hara, S.4
  • 27
    • 78049525024 scopus 로고    scopus 로고
    • The cyclic ethers (6ca and 6ca′) are separable by silica gel column chromatography, but their stereochemical identification is difficult
    • The cyclic ethers (6ca and 6ca′) are separable by silica gel column chromatography, but their stereochemical identification is difficult.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.