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Volumn 44, Issue 47, 2005, Pages 7718-7721

Oxindole synthesis through intramolecular nucleophilic addition of vinylpalladiums to aryl isocyanates

Author keywords

Alkynes; Isocyanates; Nucleophilic addition; Oxindoles; Palladium

Indexed keywords

AROMATIC COMPOUNDS; CATALYSTS; ETHANE; PALLADIUM;

EID: 28744455408     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200502252     Document Type: Article
Times cited : (74)

References (50)
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  • 7
    • 0000702671 scopus 로고
    • and references therein
    • The Heck reaction and CO-insertion reaction are representative exceptions. In the Heck reaction, organopalladium species act as weak nucleophiles toward electron-deficient olefins to give 1,4 adducts. In the case of the CO-insertion reaction, acylpalladium species are formed by insertion of CO into the C-Pd bond of organopalladium species. See: a) R. F. Heck, Org. React. 1982, 27, 345-390, and references therein;
    • (1982) Org. React. , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 9
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    • ref. [2]
    • c) ref. [2].
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    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 3208-3210
  • 34
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    • Angew. Chem. Int. Ed. 2004, 43, 1270-1272;
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    • Angew. Chem. Int. Ed. 2000, 39, 2540-2544;
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  • 49
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    • and references therein
    • For reviews on phosphine-mediated and -catalyzed reactions, see: a) X. Lu, C. Zhang, Z. Xu, Acc. Chem. Res. 2001, 34, 535-544, and references therein;
    • (2001) Acc. Chem. Res. , vol.34 , pp. 535-544
    • Lu, X.1    Zhang, C.2    Xu, Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.