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Volumn 29, Issue 11, 2010, Pages 2616-2630

Facile derivatization of a "chemo-active" NHC incorporating an enolate backbone and relevant tuning of its electronic properties

Author keywords

[No Author keywords available]

Indexed keywords

BOUND LIGANDS; CARBENE LIGANDS; CARBENES; CHLOROACETYL CHLORIDE; DERIVATIZATION OF; ELECTROPHILIC REAGENTS; ENOLATES; FORMAMIDINES; FUNCTIONALIZATIONS; FUNCTIONALIZED; IMIDAZOLIN-2-YLIDENE; IMIDAZOLIUM; METHYLENE GROUPS; N-HETEROCYCLIC CARBENE LIGANDS; NHC LIGANDS; NUCLEOPHILICITIES; SYNTHETIC ROUTES; THERMALLY INDUCED; X-RAY STRUCTURE;

EID: 77953193730     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om1003607     Document Type: Article
Times cited : (140)

References (86)
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    • For monographs, see: (Topics in Organometallic Chemistry; Vol.);, Ed.; Springer: Berlin, 2007
    • For monographs, see: N-Heterocyclic Carbenes in Transition Metal Catalysis (Topics in Organometallic Chemistry 2007; Vol. 21); Glorius, F., Ed.; Springer: Berlin, 2007
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    • For synthetic methods of NHCs, see: U.S. Patent 5 077 414
    • For synthetic methods of NHCs, see: Arduengo, A. J., III. U.S. Patent 5 077 414, 1992.
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    • (2006)
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    • For a comparison of the catalytic performances of a series of electronically identical NHCs exhibiting different steric constraints, see
    • For a comparison of the catalytic performances of a series of electronically identical NHCs exhibiting different steric constraints, see: Würtz, S.; Glorius, F. Acc. Chem. Res. 2008, 41, 1523
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1523
    • Würtz, S.1    Glorius, F.2
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    • While the present work was reviewed, a new, nice method to functionalize the backbone atoms of an unsaturated five-membered-ring NHC has appeared; see: asap, 10.1021/ja102639a
    • While the present work was reviewed, a new, nice method to functionalize the backbone atoms of an unsaturated five-membered-ring NHC has appeared; see: Mendosa-Espinosa, D.; Donnadieu, B.; Bertrand, G. J. Am. Chem. Soc. 2010, asap, 10.1021/ja102639a.
    • (2010) J. Am. Chem. Soc.
    • Mendosa-Espinosa, D.1    Donnadieu, B.2    Bertrand, G.3
  • 48
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    • For leading references on redox-active ligands and catalysts, see
    • For leading references on redox-active ligands and catalysts, see: Allgeier, A. M.; Mirkin, C. A. Angew. Chem.. Int. Ed. 1998, 37, 894
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 894
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    • See also the following related work developed by the Glorius group
    • See also the following related work developed by the Glorius group: Biju, A. T.; Hirano, K.; Fröhlich, R.; Glorius, F. Chem. Asian J. 2009, 4, 1786
    • (2009) Chem. Asian J. , vol.4 , pp. 1786
    • Biju, A.T.1    Hirano, K.2    Fröhlich, R.3    Glorius, F.4
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    • See for instance: and references therein
    • See for instance: Tapu, D.; Dixon, A.; Roe, C. Chem. Rev. 2009, 109, 3385, and references therein
    • (2009) Chem. Rev. , vol.109 , pp. 3385
    • Tapu, D.1    Dixon, A.2    Roe, C.3
  • 78
    • 73549118122 scopus 로고    scopus 로고
    • Related decarbonylation processes have already been observed in Rh(I)-carbonyl complexes incorporating poor electron donors; see
    • Related decarbonylation processes have already been observed in Rh(I)-carbonyl complexes incorporating poor electron donors; see: Bittermann, A.; Herdtweck, E.; Härter, P.; Herrmann, W. A. Organometallics 2009, 28, 6963
    • (2009) Organometallics , vol.28 , pp. 6963
    • Bittermann, A.1    Herdtweck, E.2    Härter, P.3    Herrmann, W.A.4
  • 79
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    • See also ref 11e
    • See also ref 11e.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.