메뉴 건너뛰기




Volumn 138, Issue 30, 2016, Pages 9714-9719

Directing Group in Decarboxylative Cross-Coupling: Copper-Catalyzed Site-Selective C-N Bond Formation from Nonactivated Aliphatic Carboxylic Acids

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CARBOXYLIC ACIDS; CATALYSIS; CHEMICAL BONDS; COPPER; SYNTHESIS (CHEMICAL);

EID: 84982706162     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b05788     Document Type: Article
Times cited : (69)

References (89)
  • 7
    • 84881453651 scopus 로고    scopus 로고
    • Park, K.; Lee, S. RSC Adv. 2013, 3, 14165 10.1039/c3ra41442f
    • (2013) RSC Adv. , vol.3 , pp. 14165
    • Park, K.1    Lee, S.2
  • 25
    • 0002399353 scopus 로고
    • For a selected review of aliphatic acids
    • For a selected review of aliphatic acids: Harwood, H. J. Chem. Rev. 1962, 62, 99 10.1021/cr60216a002
    • (1962) Chem. Rev. , vol.62 , pp. 99
    • Harwood, H.J.1
  • 30
    • 84863280229 scopus 로고
    • Chem. Abstr. 1940, 34, 1685.
    • (1940) Chem. Abstr. , vol.34 , pp. 1685
  • 33
  • 34
    • 0000492201 scopus 로고
    • Kochi, J. K. Science 1967, 155, 415 10.1126/science.155.3761.415
    • (1967) Science , vol.155 , pp. 415
    • Kochi, J.K.1
  • 61
    • 59049089106 scopus 로고    scopus 로고
    • For a review with the PhIO-DCM oxidant system summarized comprehensively: Zhdankin, V. V.; Stang, P. J. Chem. Rev. 2008, 108, 5299 10.1021/cr800332c
    • (2008) Chem. Rev. , vol.108 , pp. 5299
    • Zhdankin, V.V.1    Stang, P.J.2
  • 63
    • 0002603882 scopus 로고
    • Wolff, M. E. Chem. Rev. 1963, 63, 55 10.1021/cr60221a004
    • (1963) Chem. Rev. , vol.63 , pp. 55
    • Wolff, M.E.1
  • 65
    • 11344292132 scopus 로고    scopus 로고
    • For a review of natural product chemistry in drug discovery: Butler, M. S. J. Nat. Prod. 2004, 67, 2141 10.1021/np040106y
    • (2004) J. Nat. Prod. , vol.67 , pp. 2141
    • Butler, M.S.1
  • 71
    • 1042286380 scopus 로고    scopus 로고
    • Zheng, Y.; Avery, M. A. Tetrahedron 2004, 60, 2091 Detailed transformation processes of these natural products are given in the Supporting Information. 10.1016/j.tet.2003.12.048
    • (2004) Tetrahedron , vol.60 , pp. 2091
    • Zheng, Y.1    Avery, M.A.2
  • 89
    • 84932352618 scopus 로고
    • Note that Reutov group has discovered that the rearrangements of alkyl radicals via 1,2-hydrogen shift almost could not be detected compared with alkyl cations: Therefore, our reaction is most likely to take place via a radical process because no cationic rearrangement product was detected when primary carboxylic acid was employed (e.g. 2b, Table 2)
    • Note that Reutov group has discovered that the rearrangements of alkyl radicals via 1,2-hydrogen shift almost could not be detected compared with alkyl cations: Reutov, O. A. Pure Appl. Chem. 1963, 7, 203 Therefore, our reaction is most likely to take place via a radical process because no cationic rearrangement product was detected when primary carboxylic acid was employed (e.g., 2b, Table 2). 10.1351/pac196307020203
    • (1963) Pure Appl. Chem. , vol.7 , pp. 203
    • Reutov, O.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.