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Volumn 6, Issue 11, 2016, Pages 7528-7535

Catalytic transfer functionalization through shuttle catalysis

Author keywords

Alkene; Catalysis; Isodesmic reactions; Reversible; Shuttle catalysis

Indexed keywords

HYDROGENATION; OLEFINS;

EID: 85003740087     PISSN: None     EISSN: 21555435     Source Type: Journal    
DOI: 10.1021/acscatal.6b02333     Document Type: Article
Times cited : (81)

References (65)
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    • Grubbs, R. H. Handbook of Metathesis; Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany, 2003.
    • (2003) Handbook of Metathesis
    • Grubbs, R.H.1
  • 14
    • 84886773605 scopus 로고    scopus 로고
    • Some recent exciting catalytic methodologies proceeding through formal group transfer from activated cyclohexadienes or dihydropyridines have not been included because the mechanism by which the donor is activated is likely not applicable to the reverse reaction. For transfer hydrosilylation, see: (a) Simonneau, A.; Oestreich, M. Angew. Chem., Int. Ed. 2013, 52, 11905-11907.
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 11905-11907
    • Simonneau, A.1    Oestreich, M.2
  • 25
  • 34
    • 84922479719 scopus 로고    scopus 로고
    • (b) Landis, C. R. Science 2015, 347, 29-30. For an acceptor-free dehydroformylation see
    • (2015) Science , vol.347 , pp. 29-30
    • Landis, C.R.1
  • 38
    • 0033521183 scopus 로고    scopus 로고
    • Two examples of forward transfer hydroformylation are reported in the following
    • Two examples of forward transfer hydroformylation are reported in the following: Lenges, C. P.; Brookhart, M. Angew. Chem., Int. Ed. 1999, 38, 3533-3537.
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 3533-3537
    • Lenges, C.P.1    Brookhart, M.2
  • 40
    • 84936990203 scopus 로고    scopus 로고
    • Catalytic irreversible CO transfer has been reported in a Pauson-Khand reaction
    • (b) Fuentes, J. A.; Pittaway, R.; Clarke, M. L. Chem. - Eur. J. 2015, 21, 10645-10649. Catalytic irreversible CO transfer has been reported in a Pauson-Khand reaction
    • (2015) Chem. - Eur. J. , vol.21 , pp. 10645-10649
    • Fuentes, J.A.1    Pittaway, R.2    Clarke, M.L.3
  • 48
    • 84959004061 scopus 로고    scopus 로고
    • Transition metalcatalyzed alkene and alkyne hydrocyanations
    • Beller, M., Bolm, C., Eds.; Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany
    • (b) Casalnuovo, A. L.; Rajan Babu, T. V. Transition Metalcatalyzed Alkene and Alkyne Hydrocyanations. In Transition Metals for Organic Synthesis: Building Blocks and Fine Chemicals; Beller, M., Bolm, C., Eds.; Wiley-VCH Verlag GmbH and Co.: Weinheim, Germany, 2008; pp 149-156. For a method using in situ-generated HCN from TMSCN, see:.
    • (2008) Transition Metals for Organic Synthesis: Building Blocks and Fine Chemicals , pp. 149-156
    • Casalnuovo, A.L.1    Rajan Babu, T.V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.