Title of article :
Catalytic enantioselective alkenylation and phenylation of trifluoromethyl ketones
Author/Authors :
Motoki، نويسنده , , Rie and Tomita، نويسنده , , Daisuke and Kanai، نويسنده , , Motomu and Shibasaki، نويسنده , , Masakatsu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2006
Pages :
4
From page :
8083
To page :
8086
Abstract :
Catalytic enantioselective alkenylation and phenylation of trifluoromethyl ketones are described. High enantioselectivity (up to 84% ee) was produced in an alkenylation of aryl trifluoromethyl ketones using a CuF–DTBM-SEGPHOS complex as the catalyst (5–10 mol %) and alkenylsilanes as the nucleophile. This is the first example of catalytic enantioselective alkenylation of trifluoromethyl ketones. The products are versatile chiral building blocks, which contain a trifluoromethyl-substituted tertiary alcohol moiety.
Journal title :
Tetrahedron Letters
Serial Year :
2006
Journal title :
Tetrahedron Letters
Record number :
1853159
Link To Document :
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