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Volumn 47, Issue 46, 2006, Pages 8083-8086

Catalytic enantioselective alkenylation and phenylation of trifluoromethyl ketones

Author keywords

[No Author keywords available]

Indexed keywords

COPPER COMPLEX; KETONE DERIVATIVE; SILANE DERIVATIVE; TRIFLUOROMETHYLKETONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33749533572     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.09.048     Document Type: Article
Times cited : (58)

References (61)
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    • 0034327140 scopus 로고    scopus 로고
    • For asymmetric fluorination reactions using stoichiometric chiral controllers, see:
    • For asymmetric fluorination reactions using stoichiometric chiral controllers, see:. Shibata N., Suzuki E., and Takeuchi Y. J. Am. Chem. Soc. 122 (2000) 10728
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10728
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    • 11144341001 scopus 로고    scopus 로고
    • For a comprehensive review of synthetic methods of fluorine-containing molecules, see:
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    • (2004) Chem. Rev. , vol.104 , pp. 6119
    • Ma, J.-A.1    Cahard, D.2
  • 52
    • 33749531917 scopus 로고    scopus 로고
    • note
    • Preliminary optimization of the reaction solvent, chiral ligand, and additives in the phenylation reaction has not improved the enantioselectivity so far.
  • 53
    • 33746112742 scopus 로고    scopus 로고
    • For catalytic enantioselective arylation of activated ketones, see:
    • For catalytic enantioselective arylation of activated ketones, see:. Shintani R., Inoue M., and Hayashi T. Angew. Chem., Int. Ed. 45 (2006) 3353
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 3353
    • Shintani, R.1    Inoue, M.2    Hayashi, T.3
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    • For catalytic enantioselective synthesis of 5 using Sharpless dihydroxylation as a key step, see:
    • For catalytic enantioselective synthesis of 5 using Sharpless dihydroxylation as a key step, see:. Bennani Y.L., Vanhessche K.P.M., and Sharpless K.B. Tetrahedron: Asymmetry 5 (1994) 1473
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 1473
    • Bennani, Y.L.1    Vanhessche, K.P.M.2    Sharpless, K.B.3
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    • For a review of catalytic enantioselective alkynylation of ketones, see:
    • For a review of catalytic enantioselective alkynylation of ketones, see:. Pu L. Tetrahedron 59 (2003) 9873
    • (2003) Tetrahedron , vol.59 , pp. 9873
    • Pu, L.1
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    • 33749521638 scopus 로고    scopus 로고
    • During the review of this paper, Rh-catalyzed enantioselective arylation of trifluoromethyl ketones appeared: Martina, S. L. X.; Jagt, R. B. C.; de Vries, J. G.; Feringa, B. L.; Minnaard, A. J. Chem. Commun. (advanced article).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.