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Efficient Access to cis-Hydrobenzo[b]oxepines: Rhodium(I)-Catalyzed Cyclization of Cyclohexadienone-Tethered o-Tolyl-Substituted Alkynes
Synlett ( IF 2 ) Pub Date : 2018-03-14 , DOI: 10.1055/s-0036-1591956
Jia-Xin Wang 1 , Yun-Xuan Tan 2 , Wei-Wei Liao 1 , Ping Tian 2, 3 , Guo-Qiang Lin 2, 3 , Qian Zhao 4
Affiliation  

An efficient access to cis -hydrobenzo[ b ]oxepine frameworks has been established through rhodium(I)-catalyzed cyclization of cyclohexadienone-tethered o -tolyl-substituted alkynes (1,6-enynes). The cascade process involves regioselective α-arylrhodation of the alkyne, 1,4-rhodium migration, and conjugate addition to cyclohexadienone.

中文翻译:

有效获取顺式-氢苯并 [b] 氧杂环庚烷:铑(I)-催化环己二烯酮连接邻甲苯基取代炔烃的环化

通过铑(I)催化的环己二烯酮连接的邻甲苯基取代的炔烃(1,6-烯炔)的环化,已经建立了对顺式-氢苯并[b]氧杂环庚烷骨架的有效途径。级联过程涉及炔烃的区域选择性 α-芳基铑化、1,4-铑迁移和与环己二烯酮的共轭加成。
更新日期:2018-03-14
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