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An Efficient and Practical Synthesis of Dibenzo[d,f][1,3]- dioxepines from 2,2'-Dihydroxybiphenyl with Terminal Alkynes Catalyzed by Lewis Acid TiCl4

An Efficient and Practical Synthesis of Dibenzo[d,f][1,3]- dioxepines from 2,2'-Dihydroxybiphenyl with Terminal Alkynes Catalyzed by Lewis Acid TiCl4
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摘要 A synthetic strategy toward the cyclic addition of 2,2'-dihydroxybiphenyl to terminal alkynes has been developed using Lewis acid TICl4 as catalyst. The reactions generated dibenzo[d,f][1,3]dioxepines derivatives in good yields with excellent regio-selectivity in the presence of catalytic amount of TICl4 under mild reaction conditions. A synthetic strategy toward the cyclic addition of 2,2'-dihydroxybiphenyl to terminal alkynes has been developed using Lewis acid TICl4 as catalyst. The reactions generated dibenzo[d,f][1,3]dioxepines derivatives in good yields with excellent regio-selectivity in the presence of catalytic amount of TICl4 under mild reaction conditions.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第6期1211-1215,共5页 中国化学(英文版)
基金 Project supported by the National Natural Science Foundation of China (No. 20972057).
关键词 cyclic addition 2 2'-dihydroxybiphenyl terminal alkynes region-selectivity Lewis acid TICL4 cyclic addition, 2,2'-dihydroxybiphenyl, terminal alkynes, region-selectivity, Lewis acid, TICl4
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