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Volumn 8, Issue 16, 2006, Pages 3561-3564

Copper-catalyzed intermolecular hydroamination of alkenes

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EID: 33747291922     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol061355b     Document Type: Article
Times cited : (136)

References (29)
  • 17
    • 27144489030 scopus 로고    scopus 로고
    • Strong Brønsted acids catalyze competitive hydroamination and hydroarylation reactions between styrene and aniline at 135 °C: Anderson, L. L.; Arnold, J.; Bergman, R. G. J. Am. Chem. Soc. 2005, 127, 14542.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 14542
    • Anderson, L.L.1    Arnold, J.2    Bergman, R.G.3
  • 20
    • 15044358965 scopus 로고    scopus 로고
    • NBS (20 mol %) catalyzes the addition of sulfonamides to activated styrenes containing OMe or SMe groups only: Talluri, S. K.; Sudalai, A. Org. Lett. 2005, 7, 855.
    • (2005) Org. Lett. , vol.7 , pp. 855
    • Talluri, S.K.1    Sudalai, A.2
  • 21
    • 33747213174 scopus 로고    scopus 로고
    • note
    • 2 showed a mixture of crossover products (CI-MS). This could be the result of substitution reactions.
  • 22
    • 33747277536 scopus 로고    scopus 로고
    • note
    • Prepared by the tosylation of commercially available S-(-)-1- phenylethylamine.
  • 23
    • 33747323187 scopus 로고    scopus 로고
    • note
    • S = 20.4 min).
  • 25
    • 33747252007 scopus 로고    scopus 로고
    • note
    • Four equivalents of styrene were needed for the Au-catalyzed reaction, which proceeded with 51% yield in 14 h (ref 9).
  • 26
    • 33947571893 scopus 로고
    • 3J coupling is typically <1 Hz for an endo-proton and 4 Hz for an exo-proton. See: (a) Laszlo, P.; Schleyer, P. v. R. J. Am. Chem. Soc. 1964, 86, 1171-1179.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 1171-1179
    • Laszlo, P.1    Schleyer, P.V.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.