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Mn(lll)-Mediated Chlorination of Conjugated Ketones

Mn(lll)-Mediated Chlorination of Conjugated Ketones
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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.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 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).
关键词 CHLORINATION Mn(OAc)3 α β-unsaturated ketone chlorination, Mn(OAc)3, α,β-unsaturated ketone
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