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Volumn 132, Issue 50, 2010, Pages 17680-17683

Concerted C-N and C-H bond formation in a magnesium-catalyzed hydroamination

Author keywords

[No Author keywords available]

Indexed keywords

BOND FORMATION; C-H BOND; CATALYTIC CYCLES; EMPIRICAL RATE LAW; H-BONDS; HYDROAMINATIONS; LIMITING STEP; MICHAELIS-MENTEN-TYPE KINETICS; PRECATALYSTS; RESTING STATE; TRACE AMOUNTS; TRANSITION STATE; UNIMOLECULAR;

EID: 78650300023     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja108881s     Document Type: Article
Times cited : (107)

References (42)
  • 21
    • 78649889213 scopus 로고    scopus 로고
    • J. Organomet. Chem. 2010, doi: 10.1016/j.jorganchem.2010.08.057
    • Neal, S. R., Ellern, A., and Sadow, A. D. J. Organomet. Chem. 2010, doi: 10.1016/j.jorganchem.2010.08.057.
    • Neal, S.R.1    Ellern, A.2    Sadow, A.D.3
  • 26
    • 78650283961 scopus 로고    scopus 로고
    • MMgMe are 7.4 and 2 steradians, as determined by the program Solid-G using X-ray crystallographic coordinates
    • MMgMe are 7.4 and 2 steradians, as determined by the program Solid-G using X-ray crystallographic coordinates.
  • 33
    • 78650258240 scopus 로고    scopus 로고
    • See SI for kinetic analysis
    • See SI for kinetic analysis.
  • 35
    • 78650274172 scopus 로고    scopus 로고
    • A referee suggested an alternative possibility for the apparent inert nature of 12, where insertion is reversible but favors the magnesium-amido reactant. While this explanation cannot be ruled out for the stoichiometric reaction, the isotope effect and substrate saturation data, taken together, are not consistent with a reversible insertion under catalytic conditions
    • A referee suggested an alternative possibility for the apparent inert nature of 12, where insertion is reversible but favors the magnesium-amido reactant. While this explanation cannot be ruled out for the stoichiometric reaction, the isotope effect and substrate saturation data, taken together, are not consistent with a reversible insertion under catalytic conditions.
  • 37
    • 78650269591 scopus 로고    scopus 로고
    • CIFIT; Chemistry Department, McMaster University
    • Bain, A. D. CIFIT; Chemistry Department, McMaster University, 2003.
    • (2003)
    • Bain, A.D.1
  • 39
    • 78650273208 scopus 로고    scopus 로고
    • 3-coordination
    • 3-coordination.
  • 42
    • 78650293639 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed., accepted for publication
    • Manna, K., Xu, S., and Sadow, A. D. Angew. Chem., Int. Ed., accepted for publication.
    • Manna, K.1    Xu, S.2    Sadow, A.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.