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Volumn , Issue 5, 2005, Pages 889-894

The formation of 1-aryl-substituted naphthalenes by an unusual cyclization of arylethynes catalyzed by ruthenium and rhodium porphyrins

Author keywords

Catalysis; Cyclooligomerization; Metalloporphyrins; Rhodium; Ruthenium

Indexed keywords

1,2 DICHLOROBENZENE; ACETYLENE DERIVATIVE; LIGAND; NAPHTHALENE DERIVATIVE; PORPHYRIN DERIVATIVE; RHODIUM; RUTHENIUM; VINYL DERIVATIVE;

EID: 15244355559     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400746     Document Type: Article
Times cited : (29)

References (77)
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  • 12
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    • k) See article Recent Developments in Biomimetic Oxidation Catalysis by B. Meunier published in a special issue: B. Meunier, J. Mol. Catal. A: Chem. 1996, 113, 1-422.
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    • 15244352284 scopus 로고
    • Section H (Ed.: K. M. Smith), Elsevier Scientific Publishing Co., Amsterdam
    • b) J.-H. Fuhrhop, K. M. Smith, in Porphyrins and Metalloporphyrins, Section H (Ed.: K. M. Smith), Elsevier Scientific Publishing Co., Amsterdam, 1975, pp. 766-769.
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    • Fuhrhop, J.-H.1    Smith, K.M.2
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    • note
    • The type of substitution of the diphenylnaphthalene and tetraphenylbenzenes was not determined, because it was not possible to isolate the pure compounds from the reaction mixture. The yields of these compounds were low and they were produced along with the other reaction products (i.e., 1-phenyl-naphthalene and the triphenylbenzenes). As in Scheme 1, we are inclined to assign the structure of the diphenylnaphthalene as reported in Scheme 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.