An Efficient and Practical Synthesis of Dibenzo[d,f][1,3]- dioxepines from 2,2'-Dihydroxybiphenyl with Terminal Alkynes Catalyzed by Lewis Acid TiCl4
- ISSN号:1001-604X
- 期刊名称:《中国化学:英文版》
- 分类:O623.124[理学—有机化学;理学—化学] TQ134.11[化学工程—无机化工]
- 作者机构:[1]Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, China, [2]'State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
- 相关基金:Project supported by the National Natural Science Foundation of China (No. 20972057).
关键词:
末端炔烃, 四氯化钛, LEWIS酸, 催化剂, 二羟基, 二苯并, 合成, 反应条件, cyclic addition, 2,2'-dihydroxybiphenyl, terminal alkynes, region-selectivity, Lewis acid, TICl4
中文摘要:
向到终端炔属羟的 2,2-dihydroxybiphenyl 的周期的增加的合成策略作为催化剂用路易斯酸 TiCl4 被开发了。反应产生了 dibenzo [d, f ][1,3 ] 在有优秀 regio 选择的好收益的 dioxepines 衍生物面对在温和反应条件下面的 TiCl4 的催化数量。
英文摘要:
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.