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Volumn 6, Issue 5, 2011, Pages 1142-1146

Ruthenium-catalyzed one-pot aromatic secondary amine formation from nitroarenes and alcohols

Author keywords

alcohols; alkylation; nitroarenes; ruthenium; secondary amines

Indexed keywords

HIGH SELECTIVITY; NITROARENES; ONE POT; RU(ACAC); SECONDARY AMINES; TERTIARY AMINE; TRACE AMOUNTS;

EID: 79955608915     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000945     Document Type: Article
Times cited : (55)

References (107)
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    • One of the pioneer works of the ruthenium-catalyzed reaction of alcohols and amines to give secondary and tertiary amines was reported by SI. Murahashi et. al:,. For other selected examples of secondary amine formation using borrowing hydrogen methodlogy, see
    • One of the pioneer works of the ruthenium-catalyzed reaction of alcohols and amines to give secondary and tertiary amines was reported by SI. Murahashi et. al:, S. I. Murahashi, K. Kondo, T. Hakata, Tetrahedron Lett. 1982, 23, 229. For other selected examples of secondary amine formation using borrowing hydrogen methodlogy, see
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    • In some cases, chlorobenzene is used as reducing reagent. No reduction was observed in the absence of alcohol in chlorobenzene under our reaction conditions
    • In some cases, chlorobenzene is used as reducing reagent. No reduction was observed in the absence of alcohol in chlorobenzene under our reaction conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.