(Et_4N)_2[Fe_4(SPh)_10] Stimulated S_(RN)1 Reactions of α-Bromonaphth-alene with Pinacolone Carbanion  被引量:2

(Et_4N)_2[Fe_4(SPh)_10] Stimulated S_(RN)1 Reactions of α-Bromonaphth- alene with Pinacolone Carbanion

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作  者:Zhao ZHANG Ya Ling GONG Yu WANG Zhao Bin CHEN Pei Lan WANG 

机构地区:[1]Department of Chemistry,Shanxi University,Taiyuan 030006 [2]Test and Analysis Center of Shanxi University,Taiyuan 030006

出  处:《Chinese Chemical Letters》2001年第2期121-124,共4页中国化学快报(英文版)

基  金:the Natural Science Fund of Shanxi Province.

摘  要:The (Et_4N)_2[Fe_4(SPh)_10] stimulated reaction of α-bromonaphthalene with pinacolone carbanion in DMSO leads to the formation of 1-(α-naphthyl)pinacolone. The reaction is suggested in terms of SRN1 mechanism of aromatic nucleophillic substitution and has potential value in synthesis to obtain (-substituted naphthalene derivaties.The (Et_4N)_2[Fe_4(SPh)_10] stimulated reaction of α-bromonaphthalene with pinacolone carbanion in DMSO leads to the formation of 1-(α-naphthyl)pinacolone. The reaction is suggested in terms of SRN1 mechanism of aromatic nucleophillic substitution and has potential value in synthesis to obtain (-substituted naphthalene derivaties.

关 键 词:SRN1 reaction naphthalene derivative pinacolone carbanion nucleophilic substitution. 

分 类 号:O614[理学—无机化学]

 

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