Title of article :
The highly enantioselective transformation of silylketenes into α-silylthioesters catalysed by cinchona alkaloids
Author/Authors :
Blake، نويسنده , , Alexander J and Friend، نويسنده , , Christopher L and Outram، نويسنده , , Robert J and Simpkins، نويسنده , , Nigel S and Whitehead، نويسنده , , Andrew J، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2001
Pages :
5
From page :
2877
To page :
2881
Abstract :
The reaction of silylketenes with thiophenol, mediated by cinchona alkaloid catalysts, proceeds to give α-silylthioester products in good chemical yield and with enantiomeric excess values in the range 79–93%. The absolute configuration of one of the thioester products was determined by X-ray diffraction.
Journal title :
Tetrahedron Letters
Serial Year :
2001
Journal title :
Tetrahedron Letters
Record number :
1644332
Link To Document :
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