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Volumn , Issue 23, 2009, Pages 3472-3474

Direct arylation of cyclic enamides via Pd(ii)-catalyzed C-H activation

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; BENZENEBORONIC ACID; BORONIC ACID DERIVATIVE; DIOXANE; ENAMIDE DERIVATIVE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 68049127690     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b903151k     Document Type: Article
Times cited : (102)

References (36)
  • 29
    • 0028888224 scopus 로고
    • An experiment to prove path c: the ratio of the coupling products in Table 2, entry 5 (original ratio 80: 20), under standard phenylation reaction conditions for 16 h, changed to 25: 75
    • T. G. Back J. H.-L. Chau M. Parvez Synthesis 1995 162
    • (1995) Synthesis , pp. 162
    • Back, T.G.1    Chau, J.H.-L.2    Parvez, M.3
  • 30
    • 0000772583 scopus 로고
    • Aromatic acetamide 7 was observed under the reaction conditions of the direct arylation of 1 in the absence of organoboronic acid For their importance and extensive application in asymmetric catalytic hydrogenation, see:
    • H. Horino N. Inuoe J. Org. Chem. 1981 46 4416
    • (1981) J. Org. Chem. , vol.46 , pp. 4416
    • Horino, H.1    Inuoe, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.