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Volumn 11, Issue 18, 2009, Pages 4248-4250

Direct prenylation of aromatic and α,β-unsaturated carboxamides via iridium-catalyzed C-H oxidative addition-allene insertion

Author keywords

[No Author keywords available]

Indexed keywords

ALKADIENE; ALLENE; AROMATIC HYDROCARBON; IRIDIUM; OXIDIZING AGENT;

EID: 70349162922     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901759t     Document Type: Article
Times cited : (139)

References (55)
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    • For selected reviews on catalytic C-C bond formation via C-H activation initiated π-bond insertion
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    • For selected reviews of catalytic C-C bond formation via C-H activation initiated arylation
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    • 0000100584 scopus 로고    scopus 로고
    • For selected reviews of catalytic C-C bond formation via carbenoid insertion
    • For selected reviews of catalytic C-C bond formation via carbenoid insertion, see: (a) Doyle, M. P.; Forbes, D. C. Chem. Rev. 1998, 98, 911.
    • (1998) Chem. Rev. , vol.98 , pp. 911
    • Doyle, M.P.1    Forbes, D.C.2
  • 26
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    • For carbonyl reverse prenylation via indium-catalyzed hydrogenative and transfer hydrogenative coupling of 1,1-dimethylallene
    • For carbonyl reverse prenylation via indium-catalyzed hydrogenative and transfer hydrogenative coupling of 1,1-dimethylallene, see: (a) Skucas, E.; Bower, J. F.; Krische, M. J. J. Chem. Soc. 2007, 129, 12678.
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  • 29
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    • For the reverse prenylation of carboxylic acids employing 1,1-dimethylallene
    • (d) For the reverse prenylation of carboxylic acids employing 1,1-dimethylallene, see: Kim, I. S.; Krische, M. J. Org. Lett. 2008, 10, 513.
    • (2008) Org. Lett. , vol.10 , pp. 513
    • Kim, I.S.1    Krische, M.J.2
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    • 0034245863 scopus 로고    scopus 로고
    • For reviews of metal-catalyzed reactions of allenes
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    • (2000) Chem. Rev. , vol.100 , pp. 3067
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    • (c) Ma, S. Chem. Rev. 2005, 105, 2829.
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    • For iridium-catalyzed C-C bond formation via O-directed orthoC-H activation initiated p-bond insertion
    • For iridium-catalyzed C-C bond formation via O-directed orthoC-H activation initiated p-bond insertion, see: (a) Lin, Y.; Ma, D.; Lu, X. Tetrahedron Lett. 1987, 28, 3249.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 3249
    • Lin, Y.1    Ma, D.2    Lu, X.3
  • 43
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    • Stoichiometric ortho-cyclometallation of iridium centers onto m-nitrobenzoate occurs at the para-position with respect to the nitro moiety
    • Stoichiometric ortho-cyclometallation of iridium centers onto m-nitrobenzoate occurs at the para-position with respect to the nitro moiety: (a) Kisenyi, J. M.; Sunley, G. J.; Cabeza, J. A.; Smith, A. J.; Adams, H.; Salt, N. J.; Maitlis, P. M. J. Chem. Soc., Dalton Trans. 1987, 2459.
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    • See ref 2i and literature cited therein.
    • See ref 2i and literature cited therein.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.