کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5220043 | 1383376 | 2012 | 29 صفحه PDF | دانلود رایگان |
This review details the current methods used to prepare vinyl triflates derived from 1,3-dicarbonyl compounds and describes the reactivity of such functionalized vinyl triflates. α-Ketovinyl triflates can easily and stereoselectively be produced through three different ways. Enolization and triflation is the most common route, but direct triflation with triflic anhydride could also be used, each involving different mechanisms. Direct addition of triflic acid and related sulfonic acids to triple bond offers an alternative to the previous methods. With their peculiar set of functional groups, α-ketovinyl triflates can react in four different ways. The vinyl triflate part could be engaged in coupling reactions, while the carbonyl group as well as the enone motif could be subjected to nucleophilic additions. If a proton is available next to the triflate group, eliminations could occur under basic conditions. Upon addition, fragmentations could also be possible.
Journal: Tetrahedron - Volume 68, Issue 36, 9 September 2012, Pages 7245-7273