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Volumn , Issue 34, 2008, Pages 5798-5804

Iron(III)-catalyzed addition of benzylic alcohols to aryl alkynes - A new synthesis of substituted aryl ketones

Author keywords

Addition reaction; Alcohols; Alkynes; Atom economy; Ferric chloride

Indexed keywords


EID: 56749104228     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200800713     Document Type: Article
Times cited : (72)

References (53)
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    • The addition of adamantan-1-ol to acetylene, aliphatic and aromatic alkynes with sulfuric acid leads to the corresponding carbonyl compounds. For example, see: D. R. Kell, F. J. McQuillin, J. Chem. Soc. Perkin Trans. 1 1973, 2100-2103;
    • a) The addition of adamantan-1-ol to acetylene, aliphatic and aromatic alkynes with sulfuric acid leads to the corresponding carbonyl compounds. For example, see: D. R. Kell, F. J. McQuillin, J. Chem. Soc. Perkin Trans. 1 1973, 2100-2103;
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    • In dichloromethane and dichloroethane, along with a trace amount of the desired product, a reasonable amount of a vinylic chloride derivative was observed, which is currently under study
    • In dichloromethane and dichloroethane, along with a trace amount of the desired product, a reasonable amount of a vinylic chloride derivative was observed, which is currently under study.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.