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Volumn 134, Issue 37, 2012, Pages 15505-15511

Metal-free iodine(III)-promoted direct intermolecular C-H amination reactions of acetylenes

Author keywords

[No Author keywords available]

Indexed keywords

AMINATION REACTION; ARYLALKYNES; HYPERVALENT IODINE REAGENTS; SINGLE-STEP; TERMINAL ALKYNE; YNAMIDES;

EID: 84866519822     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja306211q     Document Type: Article
Times cited : (124)

References (100)
  • 10
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    • For an oxidative amination/diketonization sequence
    • For an oxidative amination/diketonization sequence: Zhang, C; Jiao, N. J. Am. Chem. Soc. 2010, 128, 28
    • (2010) J. Am. Chem. Soc. , vol.128 , pp. 28
    • Zhang, C.1    Jiao, N.2
  • 11
    • 77951780267 scopus 로고    scopus 로고
    • For decarboxylative coupling under copper catalysis, see
    • For decarboxylative coupling under copper catalysis, see: Jia, W.; Jiao, N. Org. Lett. 2010, 12, 2000
    • (2010) Org. Lett. , vol.12 , pp. 2000
    • Jia, W.1    Jiao, N.2
  • 29
    • 77954551161 scopus 로고    scopus 로고
    • For a Suzuki-type coupling, see
    • For a Suzuki-type coupling, see: Jouvin, K.; Couty, F.; Evano, G. Org. Lett. 2010, 12, 3272
    • (2010) Org. Lett. , vol.12 , pp. 3272
    • Jouvin, K.1    Couty, F.2    Evano, G.3
  • 31
    • 0032505191 scopus 로고    scopus 로고
    • For a review on the chemistry of hypervalent acetylenyl iodine(III) reagents, see
    • For a review on the chemistry of hypervalent acetylenyl iodine(III) reagents, see: Zhdankin, V. V.; Stang, P. J. Tetrahedron 1998, 54, 10927
    • (1998) Tetrahedron , vol.54 , pp. 10927
    • Zhdankin, V.V.1    Stang, P.J.2
  • 32
    • 62349110443 scopus 로고    scopus 로고
    • For a review on the corresponding bromine(III) reagents, see
    • For a review on the corresponding bromine(III) reagents, see: Ochiai, M. Synlett 2009, 159
    • (2009) Synlett , pp. 159
    • Ochiai, M.1
  • 68
    • 79955429544 scopus 로고    scopus 로고
    • For an elegant C-H amination with a preformed organonitrenoid reagent, see
    • For an elegant C-H amination with a preformed organonitrenoid reagent, see: Ochiai, M.; Miyamoto, K.; Kaneaki, T.; Hayashi, S.; Nakanishi, W. Science 2011, 332, 448
    • (2011) Science , vol.332 , pp. 448
    • Ochiai, M.1    Miyamoto, K.2    Kaneaki, T.3    Hayashi, S.4    Nakanishi, W.5
  • 92
    • 0004286484 scopus 로고    scopus 로고
    • For a discussion on the nucleophuge character of iodine(III), see: In; Akiba, K. Wiley-VCH: New York
    • For a discussion on the nucleophuge character of iodine(III), see: Ochiai, M. In Chemistry of Hypervalent Compounds; Akiba, K., Ed.; Wiley-VCH: New York, 1999; p 359.
    • (1999) Chemistry of Hypervalent Compounds , pp. 359
    • Ochiai, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.