메뉴 건너뛰기




Volumn 42, Issue 9, 2013, Pages 1076-1078

Construction of indole skeletons by sequential actions of sunlight and rhodium on α-aminoacetophenones

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84883709073     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.130463     Document Type: Article
Times cited : (15)

References (39)
  • 1
    • 37049073783 scopus 로고
    • Reviews on indole synthesis
    • Reviews on indole synthesis: G. W. Gribble, Contemp. Org. Synth. 1994, 1, 145.
    • (1994) Contemp. Org. Synth. , vol.1 , pp. 145
    • Gribble, G.W.1
  • 10
    • 0042645755 scopus 로고
    • For a review on solar energy storage by photoisomerizaiton
    • II
    • For a review on solar energy storage by photoisomerizaiton: G. Jones, II, S.-H. Chiang, P. T. Xuan, J. Photochem. 1979, 10, 1.
    • (1979) J. Photochem. , vol.10 , pp. 1
    • Jones, G.1    Chiang, S.-H.2    Xuan, P.T.3
  • 11
    • 84980113244 scopus 로고
    • For an acid-mediated reaction of anilines with 2-bromoacetophenones forming 2-arylindoles (BischlerMöhlau reaction), see
    • For an acid-mediated reaction of anilines with 2-bromoacetophenones forming 2-arylindoles (BischlerMöhlau reaction), see: a) R. Möhlau, Ber. Dtsch. Chem. Ges. 1881, 14, 171.
    • (1881) Ber. Dtsch. Chem. Ges. , vol.14 , pp. 171
    • Möhlau, R.1
  • 14
    • 37049157064 scopus 로고
    • For acid-mediated cyclization of α-aminoacetophenones affording 3-arylindoles, see
    • For acid-mediated cyclization of α-aminoacetophenones affording 3-arylindoles, see: A. F. Crowther, F. G. Mann, D. Purdie, J. Chem. Soc. 1943, 58.
    • (1943) J. Chem. Soc. , pp. 58
    • Crowther, A.F.1    Mann, F.G.2    Purdie, D.3
  • 16
    • 72149096779 scopus 로고    scopus 로고
    • For an iridium-catalyzed reaction of α-aminoacetophenones having a 3-acetylphenyl group on nitrogen forming 4-acetylindoles, see
    • For an iridium-catalyzed reaction of α-aminoacetophenones having a 3-acetylphenyl group on nitrogen forming 4-acetylindoles, see: K. Tsuchikama, Y.-k. Hashimoto, K. Endo, T. Shibata, Adv. Synth. Catal. 2009, 351, 2850.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2850
    • Tsuchikama, K.1    Hashimoto, Y.-K.2    Endo, K.3    Shibata, T.4
  • 17
    • 0011204975 scopus 로고
    • For cyclization of N-(o-iodophenyl)amino ketones, see
    • For cyclization of N-(o-iodophenyl)amino ketones, see: a) M. Kihara, Y. Iwai, Y. Nagao, Heterocycles 1995, 41, 2279.
    • (1995) Heterocycles , vol.41 , pp. 2279
    • Kihara, M.1    Iwai, Y.2    Nagao, Y.3
  • 36
    • 11844251240 scopus 로고    scopus 로고
    • For catalytic reactions involving enantioselective addition of aryland alkenylrhodium intermediates onto ketones, see
    • For catalytic reactions involving enantioselective addition of aryland alkenylrhodium intermediates onto ketones, see: a) R. Shintani, K. Okamoto, Y. Otomaru, K. Ueyama, T. Hayashi, J. Am. Chem. Soc. 2005, 127, 54.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 54
    • Shintani, R.1    Okamoto, K.2    Otomaru, Y.3    Ueyama, K.4    Hayashi, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.