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Volumn 132, Issue 39, 2010, Pages 13813-13822

Intramolecular hydroamination of unbiased and functionalized primary aminoalkenes catalyzed by a rhodium aminophosphine complex

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL CHAIN; AMINOPHOSPHINES; ELECTRON DONATION; FUNCTIONALIZED; HIGH ACTIVITY; HIGH REACTIVITY; HYDROAMINATION PRODUCTS; HYDROAMINATIONS; INTRAMOLECULAR HYDROAMINATION; LIMITING STEP; MECHANISTIC DATA; METAL CENTERS; MILD TEMPERATURES; P MODES; PROTONOLYSIS; RELATIVE RATES; RHODIUM CATALYSTS; RHODIUM COMPLEXES; ROOM TEMPERATURE; TRANSITION-METAL COMPLEX;

EID: 77957318019     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja1052126     Document Type: Article
Times cited : (118)

References (59)
  • 4
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    • Hovath, I. T., Ed.; Wiley-Interscience: Hoboken, NJ
    • Müller, T. E. In Encyclopedia of Catalysis; Hovath, I. T., Ed.; Wiley-Interscience: Hoboken, NJ, 2003; Vol. 3, pp 518 - 541.
    • (2003) Encyclopedia of Catalysis , vol.3 , pp. 518-541
    • Müller, T.E.1    Hovath, I.T.2
  • 6
    • 0033775563 scopus 로고    scopus 로고
    • Also see refs 48 and 49 for examples of biologically active tetrahydroisoquinoline heterocycles
    • O'Hagan, D. Nat. Prod. Rep. 2000, 17, 435 Also see refs 48 and 49 for examples of biologically active tetrahydroisoquinoline heterocycles
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 435
    • O'Hagan, D.1
  • 27
    • 0036298108 scopus 로고    scopus 로고
    • Ru-catalyzed olefin metathesis exemplifies the broad functional group tolerance exhibited by late-transition-metal catalysts. See
    • Ru-catalyzed olefin metathesis exemplifies the broad functional group tolerance exhibited by late-transition-metal catalysts. See: Toste, F. D., Chatterjee, A. K., and Grubbs, R. H. Pure Appl. Chem. 2002, 74, 7
    • (2002) Pure Appl. Chem. , vol.74 , pp. 7
    • Toste, F.D.1    Chatterjee, A.K.2    Grubbs, R.H.3
  • 37
    • 77957314593 scopus 로고    scopus 로고
    • There has been only one report of late-metal-catalyzed asymmetric intramolecular hydroamination of unactivated olefins. See
    • There has been only one report of late-metal-catalyzed asymmetric intramolecular hydroamination of unactivated olefins. See: Shen, X. and Buchwald, S. L. Angew. Chem. 2010, 122, 574
    • (2010) Angew. Chem. , vol.122 , pp. 574
    • Shen, X.1    Buchwald, S.L.2
  • 47
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    • See the Supporting Information for experimental details
    • See the Supporting Information for experimental details.
  • 50
    • 77957320501 scopus 로고    scopus 로고
    • One example of an α-branched aminoalkene (2-aminohex-5-ene) was reported to undergo cyclization in the presence of a zinc catalyst to give the product with low conversion (19%). See ref 21
    • One example of an α-branched aminoalkene (2-aminohex-5-ene) was reported to undergo cyclization in the presence of a zinc catalyst to give the product with low conversion (19%). See ref 21.
  • 56
    • 44649129980 scopus 로고    scopus 로고
    • L4 was synthesized from 4,5-dibromo-2,7-di- tert -butyl-9,9- dimethylxanthene and known bis(piperidinyl)chlorophosphine. See:, See the Supporting Information for experimental details
    • L4 was synthesized from 4,5-dibromo-2,7-di- tert -butyl-9,9- dimethylxanthene and known bis(piperidinyl)chlorophosphine. See: Amigues, E. J., Hardacre, C., Keane, G., and Miguad, M. E. Green Chem. 2008, 10, 660 See the Supporting Information for experimental details
    • (2008) Green Chem. , vol.10 , pp. 660
    • Amigues, E.J.1    Hardacre, C.2    Keane, G.3    Miguad, M.E.4
  • 59
    • 77957324959 scopus 로고    scopus 로고
    • note
    • 2. See ref 46.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.