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Volumn 55, Issue 21, 1999, Pages 6595-6602

A catalytic process based on sequential ortho-alkylation and vinylation of ortho-alkylaryl iodides via palladacycles

Author keywords

Arenes; Catalysis; Palladium

Indexed keywords

ACETIC ACID DERIVATIVE; ALIPHATIC COMPOUND; ALKENE; IODIDE; METHYL 2 N BUTYL 6 N PROPYLCINNAMATE; PALLADIUM; POLYCYCLIC AROMATIC COMPOUND; POLYCYCLIC AROMATIC HYDROCARBON; POTASSIUM DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 0033591166     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00293-8     Document Type: Article
Times cited : (90)

References (14)
  • 1
    • 0001538227 scopus 로고
    • Trost BM, Fleming I, editors. Pattenden, editor. Oxford: Pergamon Press
    • Tamao K. In: Trost BM, Fleming I, editors. Comprehensive Organic Synthesis, Vol. 3. Pattenden, editor. Oxford: Pergamon Press, 1991:435-480.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 435-480
    • Tamao, K.1
  • 2
    • 0000891348 scopus 로고
    • Trost BM, Fleming I, editors. Pattenden, editor. Oxford: Pergamon Press
    • Knight DW. In: Trost BM, Fleming I, editors. Comprehensive Organic Synthesis, Vol. 3. Pattenden, editor. Oxford: Pergamon Press, 1991: 481-520.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 481-520
    • Knight, D.W.1
  • 10
    • 0001368310 scopus 로고
    • Abel EW, Stone FGA, Wilkinson G, editors. Oxford: Pergamon Press
    • For palladium(IV)chemistry see: Canty AJ. In: Abel EW, Stone FGA, Wilkinson G, editors. Comprehensive Organometallic Chemistry II, Vol.9. Oxford: Pergamon Press, 1995: 225-290.
    • (1995) Comprehensive Organometallic Chemistry II , vol.9 , pp. 225-290
    • Canty, A.J.1
  • 11
    • 0013560629 scopus 로고    scopus 로고
    • This behaviour was proved by carrying out a Heck-type reaction with palladium acetate and added KI. Run 4 carried out in the presence of KI (1 mmol) gave a 31% conversion of 2-n-butyliodobenzene
    • This behaviour was proved by carrying out a Heck-type reaction with palladium acetate and added KI. Run 4 carried out in the presence of KI (1 mmol) gave a 31% conversion of 2-n-butyliodobenzene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.