کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1314479 | 1499355 | 2013 | 17 صفحه PDF | دانلود رایگان |
A variety of trifluoromethylated bi- and terphenyls were prepared by site-selective Suzuki–Miyaura cross-coupling reactions of various dihalogenated trifluoromethyl-substituted benzene derivatives. The reactions proceed with excellent site-selectivities.
A variety of trifluoromethylated di- and terphenyls were prepared by site-selective Suzuki–Miyaura cross-coupling reactions of various dihalogenated trifluoromethyl-substituted benzene derivatives. The reactions proceed with excellent site-selectivities.Figure optionsDownload as PowerPoint slideHighlights
► A variety of CF3-substituted benzene derivatives were prepared.
► The reactions proceed with very good site-selectivity.
► The selectivity is controlled by steric and electronic parameters.
► The reactions proceed in good yields.
Journal: Journal of Fluorine Chemistry - Volume 145, January 2013, Pages 18–34