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Volumn 51, Issue 4, 2012, Pages 1028-1032

Copper(I) enolate complexes in α-arylation reactions: Synthesis, reactivity, and mechanism

Author keywords

copper; cross coupling; kinetics; reaction mechanism; structure elucidation

Indexed keywords

ARYLATION REACTIONS; ARYLATIONS; COMPUTATIONAL RESULTS; CROSS-COUPLINGS; ENOLATES; IODOARENES; OXIDATIVE ADDITIONS; REACTION MECHANISM; RELATIVE REACTIVITIES; STRUCTURE ELUCIDATION;

EID: 84855991672     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106719     Document Type: Article
Times cited : (76)

References (28)
  • 14
    • 0040038447 scopus 로고
    • Complex 1 has been synthesized by a different method, but its structure remained unknown.
    • Complex 1 has been synthesized by a different method, but its structure remained unknown., R. Nast, W.-H. Lepel, Chem. Ber. 1969, 102, 3224.
    • (1969) Chem. Ber. , vol.102 , pp. 3224
    • Nast, R.1    Lepel, W.-H.2
  • 15
    • 49449125771 scopus 로고
    • I nitrophenylmethane and nitromethane complexes in which the enolate moieties were proposed to be present as the free anions were reported previously, but their structures were not defined by X-ray diffraction.
    • I nitrophenylmethane and nitromethane complexes in which the enolate moieties were proposed to be present as the free anions were reported previously, but their structures were not defined by X-ray diffraction., N. Marsich, A. Camus, J. Inorg. Nucl. Chem. 1977, 39, 275.
    • (1977) J. Inorg. Nucl. Chem. , vol.39 , pp. 275
    • Marsich, N.1    Camus, A.2
  • 27
    • 84856011284 scopus 로고
    • Compound 10 was likely formed through the oxidation of 9.
    • Compound 10 was likely formed through the oxidation of 9., P. M. Allen, U. Hess, C. S. Foote, M. M. Baizer, Synth. Commun. 1982, 12, 123.
    • (1982) Synth. Commun. , vol.12 , pp. 123
    • Allen, P.M.1    Hess, U.2    Foote, C.S.3    Baizer, M.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.