Mn(lll)-Mediated Chlorination of Conjugated Ketones  

Mn(lll)-Mediated Chlorination of Conjugated Ketones

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作  者:刘兴超 王璐 邹建平 

机构地区:[1]Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, Suzhou, Jiangsu 215123, China [2]Testing and Analysis Center of Suzhou University, Suzhou, Jiangsu 215123, China

出  处:《Chinese Journal of Chemistry》2011年第10期2097-2100,共4页中国化学(英文版)

基  金:Project supported by the National Natural Science Foundation of China (No. 20772088).

摘  要:Mn(III)-Cl formed by the reaction of Mn(OAc)3 and hydrochloric acid in situ, reacted with α,β-unsaturated ketones readily to afford α,β-dichloroketones in good yields under mild conditions. The products are key precursors for synthesis of conjugated alkynones and other organic compounds.Mn(III)-Cl formed by the reaction of Mn(OAc)3 and hydrochloric acid in situ, reacted with α,β-unsaturated ketones readily to afford α,β-dichloroketones in good yields under mild conditions. The products are key precursors for synthesis of conjugated alkynones and other organic compounds.

关 键 词:CHLORINATION Mn(OAc)3 α β-unsaturated ketone 

分 类 号:O625.42[理学—有机化学] O152.1[理学—化学]

 

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