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Volumn , Issue 17, 2006, Pages 3791-3802

Effects of ionic liquids on Pd-catalysed carbon-carbon bond formation

Author keywords

Carbene ligands; Carbonylation; Heck reaction; Ionic liquids; Palladium; Suzuki reaction

Indexed keywords


EID: 33748593915     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200600045     Document Type: Short Survey
Times cited : (88)

References (196)
  • 2
    • 0347417134 scopus 로고    scopus 로고
    • b) T. Welton, Chem. Rev. 1999, 99, 2071-2084;
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2084
    • Welton, T.1
  • 7
    • 0000633011 scopus 로고
    • Eds.: B. M. Trost, I. Fleming, Pergamon, Oxford
    • a) R. F. Heck, in Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming), vol. 4, Pergamon, Oxford, 1991, p. 833;
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 833
    • Heck, R.F.1
  • 63
    • 12944304643 scopus 로고    scopus 로고
    • For the Heck coupling of electron-rich olefins, see: e) J. Mo, L. Xu, J. Xiao, J. Am. Chem. Soc. 2005, 127, 751-760;
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 751-760
    • Mo, J.1    Xu, L.2    Xiao, J.3
  • 82
    • 37049081134 scopus 로고
    • For regioselective synthesis of aryl-substituted allylic alcohols see: a) T. Jeffery, J. Chem. Soc., Chem. Commun. 1991, 324-325;
    • (1991) J. Chem. Soc., Chem. Commun. , pp. 324-325
    • Jeffery, T.1
  • 90
    • 33748623966 scopus 로고    scopus 로고
    • [2]
    • [2].
  • 93
    • 4244187012 scopus 로고
    • (Pfizer Inc.), U. S. Pat. US 4,342,781 1982
    • S. B. Kadin (Pfizer Inc.), U. S. Pat. US 4,342,781 1982; Chem. Abstr. 1982, 97, 215790w.
    • (1982) Chem. Abstr. , vol.97
    • Kadin, S.B.1
  • 112
    • 33748629277 scopus 로고    scopus 로고
    • Ed.: F. E. Herkes, Marcel Dekker, New York, chapter 33
    • A. Eisestadt, in Catalysis of Organic Reactions (Ed.: F. E. Herkes), Marcel Dekker, New York, 1998, chapter 33.
    • (1998) Catalysis of Organic Reactions
    • Eisestadt, A.1
  • 125
    • 33748585836 scopus 로고    scopus 로고
    • note
    • This result is probably due to the benzylic hydrogen, whose acidity inhibits further arylation into the doubly arylated product 12 by favouring a fast isomerisation of the terminal olefin.
  • 126
    • 33748615032 scopus 로고    scopus 로고
    • note
    • a values of acetate and pivalate anions in TBAA and TBAP, respectively, cannot be the same as those measured in water. This is not be surprising, since the anions are poorly solvated in these ionic liquids and should therefore be both good ligands for palladium and strong bases.
  • 140
    • 0004126382 scopus 로고    scopus 로고
    • Ed.: J. André, National Taiwan Ocean University, Keelung, Taiwan
    • A. Domare, G. A. F. Roberts, Advances in Chitin Science (Ed.: J. André), National Taiwan Ocean University, Keelung, Taiwan 1998.
    • (1998) Advances in Chitin Science
    • Domare, A.1    Roberts, G.A.F.2
  • 152
  • 161
    • 21844453195 scopus 로고    scopus 로고
    • For a review on ion pairing in organometallic chemistry see: A. Macchioni, Chem. Rev. 2005, 105, 2039-2073.
    • (2005) Chem. Rev. , vol.105 , pp. 2039-2073
    • Macchioni, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.