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Volumn 53, Issue 27, 2014, Pages 7028-7032

Chemoselective amination of propargylic C(sp3)-H bonds by cobalt(II)-based metalloradical catalysis

Author keywords

alkynes; chemoselectivity; cobalt; heterocycles; homogeneous catalysis

Indexed keywords

BYPRODUCTS; CATALYSIS; COBALT; REACTION KINETICS;

EID: 84903318118     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201400557     Document Type: Article
Times cited : (137)

References (92)
  • 6
  • 36
    • 84866973652 scopus 로고    scopus 로고
    • 3-coupling using unactivated ketones to form quaternary-carbon-containing propargylamines, see
    • 3-coupling using unactivated ketones to form quaternary-carbon-containing propargylamines, see
    • (2012) Green Chem. , vol.14 , pp. 2672-2676
    • Pierce, C.J.1    Larsen, C.H.2
  • 39
    • 84870560725 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 12289-12292
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 12289-12292
  • 49
    • 33749864321 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 6422-6425
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 6422-6425
  • 51
    • 20644471624 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3518-3520
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3518-3520
  • 56
    • 84878049343 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 5836-5839.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 5836-5839
  • 57
    • 84855485317 scopus 로고    scopus 로고
    • 2-catalyzed intermolecular propargylic C-H amination using 1-aryl-1-butynes as substrates and N-mesyloxycarbamate as the nitrene source, see
    • 2-catalyzed intermolecular propargylic C-H amination using 1-aryl-1-butynes as substrates and N-mesyloxycarbamate as the nitrene source, see
    • (2012) Org. Lett. , vol.14 , pp. 280-283
    • Grigg, R.D.1    Rigoli, J.W.2    Pearce, S.D.3    Schomaker, J.M.4
  • 65
    • 78650429673 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 10192-10196
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 10192-10196
  • 73
    • 79961157892 scopus 로고    scopus 로고
    • for related DFT studies on the radical mechanism of [Co(Por)]-catalyzed olefin aziridination, see
    • V. Lyaskovskyy, A. I. Olivos Suarez, H. J. Lu, H. L. Jiang, X. P. Zhang, B. de Bruin, J. Am. Chem. Soc. 2011, 133, 12264-12273; for related DFT studies on the radical mechanism of [Co(Por)]-catalyzed olefin aziridination, see
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 12264-12273
    • Lyaskovskyy, V.1    Olivos Suarez, A.I.2    Lu, H.J.3    Jiang, H.L.4    Zhang, X.P.5    De Bruin, B.6
  • 75
    • 79958196432 scopus 로고    scopus 로고
    • for detailed studies on the similar radical mechanism involving cobalt(III)/carbene radical intermediates, see
    • K. H. Hopmann, A. Ghosh, ACS Catal. 2011, 1, 597-600; for detailed studies on the similar radical mechanism involving cobalt(III)/carbene radical intermediates, see
    • (2011) ACS Catal. , vol.1 , pp. 597-600
    • Hopmann, K.H.1    Ghosh, A.2
  • 85
    • 70349782195 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 2777-2779.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 2777-2779
  • 86
    • 84887010336 scopus 로고    scopus 로고
    • For one of the most versatile methods for preparation of quaternary amines, see.
    • For one of the most versatile methods for preparation of quaternary amines, see:, H. Xu, S. Chowdhury, J. A. Ellman, Nat. Protoc. 2013, 8, 2271-2280.
    • (2013) Nat. Protoc. , vol.8 , pp. 2271-2280
    • Xu, H.1    Chowdhury, S.2    Ellman, J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.