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Volumn 55, Issue 33, 2016, Pages 9676-9679

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids

Author keywords

decarboxylation; homogeneous catalysis; nickel catalysts; redox active esters; Suzuki cross coupling

Indexed keywords

CARBOXYLATION; CARBOXYLIC ACIDS; CATALYSTS; ESTERS; NICKEL; NICKEL COMPOUNDS; REDOX REACTIONS;

EID: 84979074178     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201605463     Document Type: Article
Times cited : (168)

References (41)
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    • As mentioned in ref. [3], redox-active esters are analogous to alkyl halides, a mechanistic parallel can be directly drawn to pioneering work in the area of Ni-catalyzed single-electron transfer cross-coupling of those species, se
    • As mentioned in ref. [3], redox-active esters are analogous to alkyl halides. Thus, a mechanistic parallel can be directly drawn to pioneering work in the area of Ni-catalyzed single-electron transfer cross-coupling of those species, see:
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    • For selected examples of Ni-catalyzed alkyl- -aryl Suzuki–Miyaura cross-couplings, se
    • For selected examples of Ni-catalyzed alkyl- -aryl Suzuki–Miyaura cross-couplings, see:
  • 30
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    • See Supporting Information for details
    • See Supporting Information for details.
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    • For an older route involving Friedel–Crafts of benzene with cyclohexene followed by bromination, se
    • K. Ueda, H. Umihara, S. Yokoshima, T. Fukuyama, Org. Lett. 2015, 17, 3191; For an older route involving Friedel–Crafts of benzene with cyclohexene followed by bromination, see:
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    • Ueda, K.1    Umihara, H.2    Yokoshima, S.3    Fukuyama, T.4
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    • Recently, the formation of hydroxy-bridged species between a boronate and the metal center have disclosed as key step for transmetalation in Suzuki cross-couplings with P
    • Recently, the formation of hydroxy-bridged species between a boronate and the metal center have disclosed as key step for transmetalation in Suzuki cross-couplings with Pd: A. A. Thomas, S. E. Denmark, Science 2016, 352, 329.
    • (2016) Science , vol.352 , pp. 329
    • Thomas, A.A.1    Denmark, S.E.2
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    • The capture of similar radicals was also invoked during the decarboxylative coupling of α-heteroatom stabilized acids with aryl halide
    • The capture of similar radicals was also invoked during the decarboxylative coupling of α-heteroatom stabilized acids with aryl halides: Z. Zuo, D. T. Ahneman, L. Chu, J. A. Terrett, A. G. Doyle, D. W. C. MacMillan, Science 2014, 345, 437.
    • (2014) Science , vol.345 , pp. 437
    • Zuo, Z.1    Ahneman, D.T.2    Chu, L.3    Terrett, J.A.4    Doyle, A.G.5    MacMillan, D.W.C.6
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    • This reaction is currently being enlisted at Bristol-Myers Squibb in several ongoing programs, including one involving the co-authors (B, V. and S.A.S.)
    • This reaction is currently being enlisted at Bristol-Myers Squibb in several ongoing programs, including one involving the co-authors (B.V. and S.A.S.).
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    • X-ray information for compound 17 can be obtained free of charge from The, Crystallographic Data center with number CCDC 1477360
    • X-ray information for compound 17 can be obtained free of charge from The Cambridge Crystallographic Data center with number CCDC 1477360.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.