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Volumn 9, Issue 26, 2007, Pages 5413-5416

Indium - Copper-mediated barbier - Grignard-type alkylation reaction of imines in aqueous media

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; IMINE; INDIUM; WATER;

EID: 38349173925     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702263b     Document Type: Article
Times cited : (51)

References (42)
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  • 2
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    • Trost, B. M, Fleming, I, Eds, Pergamon Press: Oxford, UK, Chapter 1.12, pp, and references cited therein
    • (b) Volkmann, R. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, UK, 1991; Vol. 1, Chapter 1.12, pp 355, and references cited therein.
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 355
    • Volkmann, R.A.1
  • 8
    • 33846515075 scopus 로고    scopus 로고
    • Allylation of imines in aqueous media is mostly limited to activated imines, such as sulfonimines, tosyl and aryl hydrazones, glyoxylic oxime ethers, etc. For examples, see: a, 28, 139 and references cited therein
    • Allylation of imines in aqueous media is mostly limited to activated imines, such as sulfonimines, tosyl and aryl hydrazones, glyoxylic oxime ethers, etc. For examples, see: (a) Piao, X.; Jung, J. K.; Knag, H. Y. Bull. Korean Chem. Soc. 2007, 28, 139 and references cited therein.
    • Bull. Korean Chem. Soc , vol.2007
    • Piao, X.1    Jung, J.K.2    Knag, H.Y.3
  • 17
    • 34447131678 scopus 로고    scopus 로고
    • Organic reactions in water; for reviews, see: a
    • Organic reactions in water; for reviews, see: (a) Herrerías, C. I.; Yao, X. Q.; Li, Z. P.; Li, C. J. Chem. Rev. 2007, 107, 2546.
    • (2007) Chem. Rev , vol.107 , pp. 2546
    • Herrerías, C.I.1    Yao, X.Q.2    Li, Z.P.3    Li, C.J.4
  • 21
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    • Yamamoto, H, Ed, Georg Thieme Verlag: New York
    • (e) Loh, T. P. In Science of Synthesis; Yamamoto, H., Ed.; Georg Thieme Verlag: New York, 2004; p 413.
    • (2004) Science of Synthesis , pp. 413
    • Loh, T.P.1
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    • (g) Li, C. J. Chem. Rev. 2005, 105, 3095.
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    • Li, C.J.1
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    • For reviews, see: a, and references cited therein
    • For reviews, see: (a) Miyabe, H.; Ueda, M.; Naito, T. Synlett 2004, 1140 and references cited therein.
    • (2004) Synlett , pp. 1140
    • Miyabe, H.1    Ueda, M.2    Naito, T.3
  • 37
    • 0037427242 scopus 로고    scopus 로고
    • For the alkylation of aldehydes in aqueous media, see
    • For the alkylation of aldehydes in aqueous media, see: Keh, C. C. K.; Wei, C. M.; Li, C. J. J. Am. Chem. Soc. 2003, 125, 4062.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 4062
    • Keh, C.C.K.1    Wei, C.M.2    Li, C.J.3
  • 39
    • 38349089498 scopus 로고    scopus 로고
    • For primary iodide and tertiary iodide, the one-pot reactions of benzaldehyde, aniline, and n-hexyl iodide or fert-butyl iodide proceeded sluggishly under optimized conditions to give the desired products in very low yields.
    • For primary iodide and tertiary iodide, the one-pot reactions of benzaldehyde, aniline, and n-hexyl iodide or fert-butyl iodide proceeded sluggishly under optimized conditions to give the desired products in very low yields.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.