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Volumn 44, Issue 24, 2005, Pages 3703-3706

Enantioselective formation of stereogenic carbon - Fluorine centers by a simple catalytic method

Author keywords

Aldehydes; Asymmetric catalysis; Electrophilic substitution; Enantioselectivity; Organocatalysis

Indexed keywords

ALCOHOLS; ALDEHYDES; CARBON; CATALYSIS; REACTION KINETICS;

EID: 20444441594     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200500395     Document Type: Article
Times cited : (442)

References (53)
  • 20
    • 0037148980 scopus 로고    scopus 로고
    • For an organocatalyzed approach, see: D. Y. Kim, E. J. Park. Org. Lett. 2002, 4, 545.
    • (2002) Org. Lett. , vol.4 , pp. 545
    • Kim, D.Y.1    Park, E.J.2
  • 28
    • 0842343649 scopus 로고    scopus 로고
    • For examples of C-O bond formation, see: a) G. Zhong, Angew. Chem. 2003, 115, 4379;
    • (2003) Angew. Chem. , vol.115 , pp. 4379
    • Zhong, G.1
  • 49
    • 20444457866 scopus 로고    scopus 로고
    • JP 62093248, JP 04024556, US 4798680, US 4873018, 1989
    • For a representative patent, see: H. Nohira, M. Kamei, S. Nakamura, K. Yoshinaga, M. Kai, JP 62093248, JP 04024556, US 4798680, US 4873018, 1989.
    • Nohira, H.1    Kamei, M.2    Nakamura, S.3    Yoshinaga, K.4    Kai, M.5
  • 53
    • 17144415210 scopus 로고    scopus 로고
    • Note added in proof (April 26, 2005): After the submission of this paper. Enders and Hüttl published the fluorination of carbonyl compounds catalyzed by chiral amines with Selectfluor as the fluorine source. The highest enantioselectivity was obtained for cyclohexanone (36% ee): D. Enders, M. R. M. Hüttl, Synlett 2005, 991.
    • (2005) Synlett , pp. 991
    • Enders, D.1    Hüttl, M.R.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.