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Volumn 51, Issue 15, 2010, Pages 2004-2006

Direct C-3 arylation of N-acetylindoles with anisoles using phenyliodine bis(trifluoroacetate) (PIFA)

Author keywords

[No Author keywords available]

Indexed keywords

ANISOLE DERIVATIVE; INDOLE DERIVATIVE; PHENYLIODINE BIS(TRIFLUOROACETATE); TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG;

EID: 77649271867     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.02.022     Document Type: Article
Times cited : (35)

References (44)
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    • For recent reviews on the synthesis of indoles, see:
    • For recent reviews on the synthesis of indoles, see:. Ackermann L. Synlett (2007) 507
    • (2007) Synlett , pp. 507
    • Ackermann, L.1
  • 19
    • 64549092935 scopus 로고    scopus 로고
    • For recent reviews of hypervalent iodine chemistry, see:
    • For recent reviews of hypervalent iodine chemistry, see:. Uyanik M., and Ishihara K. Chem. Commun. (2009) 2086
    • (2009) Chem. Commun. , pp. 2086
    • Uyanik, M.1    Ishihara, K.2
  • 23
    • 35348831379 scopus 로고    scopus 로고
    • Chapter 31.4.1
    • Zhdankin V.V. Sci. Synth. 31a (2007) 161 Chapter 31.4.1
    • (2007) Sci. Synth. , vol.31 a , pp. 161
    • Zhdankin, V.V.1
  • 27
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    • Wirth T. (Ed), Springer, Berlin
    • In: Wirth T. (Ed). Hypervalent Iodine Chemistry (2003), Springer, Berlin
    • (2003) Hypervalent Iodine Chemistry
  • 29
    • 67649496359 scopus 로고    scopus 로고
    • For recent examples of hypervalent iodine reagents in oxidative C-C bonds formation reaction, see:
    • For recent examples of hypervalent iodine reagents in oxidative C-C bonds formation reaction, see:. Liang J., Chen J., Du F., Zeng X., Li L., and Zhang H. Org. Lett. 11 (2009) 2820
    • (2009) Org. Lett. , vol.11 , pp. 2820
    • Liang, J.1    Chen, J.2    Du, F.3    Zeng, X.4    Li, L.5    Zhang, H.6
  • 43
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    • note
    • 2 and generate a reactive cationic iodine(III) intermediate. See Ref. 13b and references cited therein.
  • 44
    • 77649275357 scopus 로고    scopus 로고
    • note
    • Most of starting 2-methoxycarbonylanisole (2g) was recovered and N-acetylindole (1a) was slowly decomposed during the extended reaction times or at the elevated temperatures.


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