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Volumn 12, Issue 10, 2010, Pages 2306-2309

α-arylation of 3-aryloxindoles

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE DERIVATIVE; ORGANOMETALLIC COMPOUND; PALLADIUM;

EID: 77952357159     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100666v     Document Type: Article
Times cited : (44)

References (51)
  • 2
    • 77952327985 scopus 로고    scopus 로고
    • For current reviews of 3,3-disubstituted oxindole related natural products, see:
    • For current reviews of 3,3-disubstituted oxindole related natural products, see:
  • 7
    • 77952388729 scopus 로고    scopus 로고
    • For biological active 3,3-diaryloxindoles, see
    • For biological active 3,3-diaryloxindoles, see
  • 10
    • 77952356746 scopus 로고    scopus 로고
    • For selected recent examples of the synthesis of 3,3-disubstitued oxindoles, see:
    • For selected recent examples of the synthesis of 3,3-disubstitued oxindoles, see:
  • 24
    • 77952335479 scopus 로고    scopus 로고
    • For recent reviews of α-arylations, see
    • For recent reviews of α-arylations, see
  • 30
    • 77952324140 scopus 로고    scopus 로고
    • For the synthesis of diazonamide A, see
    • For the synthesis of diazonamide A, see
  • 39
    • 77952330300 scopus 로고    scopus 로고
    • note
    • 3 was not beneficial, even after 5 h. In both these reactions, Pd black was observed, suggesting that no active catalyst remained in solution.
  • 42
    • 77952378216 scopus 로고    scopus 로고
    • For examples of α-arylations of ketones, see ref 7
    • For examples of α-arylations of ketones, see ref 7.
  • 46
    • 77952325133 scopus 로고    scopus 로고
    • For alkylation and acylation of 3-phenyloxindole (7), see
    • For alkylation and acylation of 3-phenyloxindole (7), see
  • 48
    • 77952346772 scopus 로고    scopus 로고
    • This reaction also proceeds with protected oxindoles. For an example, see ref 11g
    • This reaction also proceeds with protected oxindoles. For an example, see ref 11g.
  • 49
    • 77952400237 scopus 로고    scopus 로고
    • note
    • 3 we were able to obtain the desired product in 61% yield along with 31% recovered 7 after 12 h at reflux.
  • 50
    • 77952367657 scopus 로고    scopus 로고
    • NAr reactions of halo-oxazoles, see
    • NAr reactions of halo-oxazoles, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.