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Volumn 136, Issue 15, 2014, Pages 5587-5590

Nickel-catalyzed reductive and borylative cleavage of aromatic carbon-nitrogen bonds in N-aryl amides and carbamates

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; NICKEL;

EID: 84899023842     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja501649a     Document Type: Article
Times cited : (162)

References (39)
  • 3
    • 84871368115 scopus 로고    scopus 로고
    • 3)-N bond cleavage is also an interesting subject
    • refs therein
    • 3)-N bond cleavage is also an interesting subject J. Am. Chem. Soc. 2012, 134, 20230 and refs therein
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 20230
    • Geng, W.1    Zhang, W.-X.2    Hao, W.3    Xi, Z.4
  • 34
    • 84859121216 scopus 로고    scopus 로고
    • The origin of the incorporated hydrogen is reported to be sensitive to the nature of the reducing agents employed in nickel-catalyzed reductive cleavage of C-O bonds
    • See also refs 7a-7c
    • Kelley, P.; Lin, S.; Edouard, G.; Day, M. W.; Agapie, T. The origin of the incorporated hydrogen is reported to be sensitive to the nature of the reducing agents employed in nickel-catalyzed reductive cleavage of C-O bonds J. Am. Chem. Soc. 2012, 134, 5480 See also refs 7a-7c
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 5480
    • Kelley, P.1    Lin, S.2    Edouard, G.3    Day, M.W.4    Agapie, T.5
  • 35
    • 84869431962 scopus 로고    scopus 로고
    • Hydrogen exchange between a nickel-hydride complex and benzene
    • Hydrogen exchange between a nickel-hydride complex and benzene: Beck, R.; Shoshani, M.; Johnson, S. A. Angew. Chem., Int. Ed. 2012, 51, 11753
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 11753
    • Beck, R.1    Shoshani, M.2    Johnson, S.A.3
  • 38
    • 84887976157 scopus 로고    scopus 로고
    • It is also probable that different metal species are present in the catalytic reaction mixture, and several of them are responsible for the catalysis
    • It is also probable that different metal species are present in the catalytic reaction mixture, and several of them are responsible for the catalysis: Kashin, A. S.; Ananikov, V. P. J. Org. Chem. 2013, 78, 11117
    • (2013) J. Org. Chem. , vol.78 , pp. 11117
    • Kashin, A.S.1    Ananikov, V.P.2
  • 39
    • 84856023500 scopus 로고    scopus 로고
    • A general aspect of nanoparticle-catalyzed cross-coupling reactions
    • A general aspect of nanoparticle-catalyzed cross-coupling reactions: Pérez-Lorenzo, M. J. Phys. Chem. Lett. 2012, 3, 167
    • (2012) J. Phys. Chem. Lett. , vol.3 , pp. 167
    • Pérez-Lorenzo, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.