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Volumn 18, Issue 13, 2012, Pages 3831-3834

A general and efficient palladium-catalyzed alkoxycarbonylation of phenols to form esters through in situ formed aryl nonaflates

Author keywords

aryl nonaflate; carbonylation; esters; palladium; phenols

Indexed keywords

ALKOXYCARBONYLATION; ARYL NONAFLATE; FERROCENES; IN-SITU; PALLADIUM-CATALYZED;

EID: 84858992988     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201103797     Document Type: Article
Times cited : (25)

References (57)
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    • 77957348920 scopus 로고    scopus 로고
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    • 0345736841 scopus 로고    scopus 로고
    • (Ed.: Z. Rappoport), Wiley, New York
    • The Chemistry of Phenols (Ed.:, Z. Rappoport,), Wiley, New York, 2003
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    • 78449240335 scopus 로고    scopus 로고
    • for a recent review on the use of mesylates, see
    • Angew. Chem. Int. Ed. 2010, 49, 8918-8922; for a recent review on the use of mesylates, see
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 8918-8922
  • 48
    • 72149085991 scopus 로고    scopus 로고
    • For an excellent review on the application of nonaflate, see.
    • For an excellent review on the application of nonaflate, see:, J. Högermeier, H. U. Reissig, Adv. Synth. Catal. 2009, 351, 2747-2763.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2747-2763
    • Högermeier, J.1    Reissig, H.U.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.