메뉴 건너뛰기




Volumn 53, Issue 19, 2014, Pages 4930-4934

Well-defined four-coordinate iron(ii) complexes for intramolecular hydroamination of primary aliphatic alkenylamines

Author keywords

alkenes; amines; homogeneous catalysis; hydroamination; iron

Indexed keywords

AMINES; CATALYSIS; HYDROCARBONS; IRON; IRON COMPOUNDS; OLEFINS; REACTION KINETICS;

EID: 84899965804     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201402089     Document Type: Article
Times cited : (64)

References (62)
  • 4
    • 84899992431 scopus 로고    scopus 로고
    • (Eds.: K. Banert, E. M. Carreira, I. Marek, H.-U. Reissig, P. G. Steel), Thieme, Stuttgart
    • J. Hannedouche, in Science of Synthesis Knowledge Update 2013/4 (Eds.:, K. Banert, E. M. Carreira, I. Marek, H.-U. Reissig, P. G. Steel,), Thieme, Stuttgart, 2013, pp. 1-126.
    • (2013) Science of Synthesis Knowledge Update 2013/4 , pp. 1-126
    • Hannedouche, J.1
  • 11
    • 54249145292 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 5302-5306
    • (2008) Angew. Chem. , vol.120 , pp. 5302-5306
  • 14
    • 84857928276 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 10093-10096
    • (2011) Angew. Chem. , vol.123 , pp. 10093-10096
  • 16
    • 84867536873 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 5265-5268.
    • (2012) Angew. Chem. , vol.124 , pp. 5265-5268
  • 21
    • 77957314593 scopus 로고    scopus 로고
    • Angew. Chem. 2010, 122, 574-577.
    • (2010) Angew. Chem. , vol.122 , pp. 574-577
  • 26
    • 33744956342 scopus 로고    scopus 로고
    • Angew. Chem. 2005, 117, 7972-7976
    • (2005) Angew. Chem. , vol.117 , pp. 7972-7976
  • 37
    • 54849171100 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 3363-3367
    • (2008) Angew. Chem. , vol.120 , pp. 3363-3367
  • 40
    • 34250612841 scopus 로고    scopus 로고
    • Angew. Chem. 2006, 118, 3004-3007
    • (2006) Angew. Chem. , vol.118 , pp. 3004-3007
  • 50
    • 84899897630 scopus 로고    scopus 로고
    • CCDC 909964 (1), 909965 (2a THF) and 909963 (2b) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 58
    • 84893577988 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 8668-8684.
    • (2013) Angew. Chem. , vol.125 , pp. 8668-8684
  • 60
    • 0001043787 scopus 로고
    • For cyclohydroamination rate depression upon the addition of non cyclizable amine:, M. R. Gagne, C. L. Stern, T. J. Marks, J. Am. Chem. Soc. 1992, 114, 275-294.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 275-294
    • Gagne, M.R.1    Stern, C.L.2    Marks, T.J.3
  • 61
    • 84863938087 scopus 로고    scopus 로고
    • For a recent discussion of σ-insertive and non-insertive mechanistic pathways for catalysts proceeding by amine activation:, S. Tobisch, Dalton Trans. 2012, 41, 9182-9191.
    • (2012) Dalton Trans. , vol.41 , pp. 9182-9191
    • Tobisch, S.1
  • 62
    • 0346994923 scopus 로고    scopus 로고
    • β-H elimination might liberate an enamine that tautomerizes to imine 5 generating {Fe-H} species. These might either insert into the C=C bond of 3 to form 6 after aminolysis or act as a Brönsted base to give A or 2c. For examples of low-coordinate β-diketiminatoiron(II) hydride and their insertion into double bond; see, J. M. Smith, R. J. Lachicotte, P. L. Holland, J. Am. Chem. Soc. 2003, 125, 15752-15753; For {Fe-H} acting as a base; see Reference [11b].
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 15752-15753
    • Smith, J.M.1    Lachicotte, R.J.2    Holland, P.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.