Title of article
A C–C bond formation reaction at the α-carbon atom of α-oxo ketene dithioacetals via the Baylis–Hillman type reaction
Author/Authors
Yin، نويسنده , , Yan-Bing and Wang، نويسنده , , Mang and Liu، نويسنده , , Qun and Hu، نويسنده , , Jiang-Lei and Sun، نويسنده , , Shao-Guang and Kang، نويسنده , , Jing، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
4399
To page
4402
Abstract
The first example of TiCl4-mediated Baylis–Hillman type reaction of α-acetyl cyclic ketene dithioacetals with arylaldehydes was described. This methodology adds a new entry to the C–C bond formation at the α-carbon atom of α-oxo ketene dithioacetals.
Keywords
activated alkenes , Baylis–Hillman type reaction , Double Baylis–Hillman products , C–C bond formation , ?-Oxo ketene dithioacetals
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1845999
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