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Volumn 55, Issue 45, 2016, Pages 14106-14110

Nickel- and Photoredox-Catalyzed Cross-Coupling Reactions of Aryl Halides with 4-Alkyl-1,4-dihydropyridines as Formal Nucleophilic Alkylation Reagents

Author keywords

cross coupling; C C cleavage; dihydropyridines; nickel catalysts; photoredox catalysts

Indexed keywords

ALKYLATION; CARBON; CATALYSIS; METAL HALIDES; NICKEL; ORGANOMETALLICS;

EID: 84992456247     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201606513     Document Type: Article
Times cited : (172)

References (88)
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    • For thermal reactions of aryl halides with aliphatic carboxylic acids (or carboxylates), see:
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    • All redox potentials in this manuscript are given in volts versus the saturated calomel electrode (V vs. SCE). The reported values versus different reference electrodes were corrected according to a literature method
    • All redox potentials in this manuscript are given in volts versus the saturated calomel electrode (V vs. SCE). The reported values versus different reference electrodes were corrected according to a literature method: V. V. Pavlishchuk, A. W. Addison, Inorg. Chim. Acta 2000, 298, 97.
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    • The rapid electron transfer between excited-state, fac, -[Ir(ppy),] and 2 a was confirmed by Stern–Volmer analysis (see the Supporting Information).
    • 3] and 2 a was confirmed by Stern–Volmer analysis (see the Supporting Information).
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    • See the Supporting Information for experimental details.
    • See the Supporting Information for experimental details.
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    • For the transformation from D to B in Scheme 5, we can not exclude the possibility that Ni, is not involved as a reactive intermediate (see Ref. [17e]).
    • 0 is not involved as a reactive intermediate (see Ref. [17e]).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.