Site-Selective Suzuki-Miyaura Reactions of 1,4-and 3,5-Bis(trifluoromethylsulfonyloxy)-2-naphthoates

[摘要]：The Suzuki-Miyaura reaction of phenyl 1,4-bis(trifluoromethylsulfonyloxy)-2-naphthoate and ethyl 3,5-bis(trifluoromethylsulfonyloxy)-2-naphthoate afforded various 1,4- and 3,5-diaryl-2- naphthoates with very good site-selectivity, respectively. The first attack occurred at the sterically more hindered positions C-1 and C-3, respectively. The selectivity can be explained by the electronic influence of the ester group.

[全文传递流程]：

一般上传文献全文的时限在1个工作日内