Title of article
An efficient preparation of stereospecific β-hydroxy nitriles
Author/Authors
Jacobo، نويسنده , , Sheila H. and Adiyaman، نويسنده , , Mustafa and Chang، نويسنده , , Chih-Tsung and Kang، نويسنده , , Nam-In and Powell، نويسنده , , William S. and Rokach، نويسنده , , Joshua، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
161
To page
164
Abstract
The cyanide-ring opening of thionocarbonates with NaCN in DMF and TBACN in THF is described. This reaction occurred regioselectively to afford β-hydroxy nitrile with preserved stereochemistry of the hydroxy group in high yield.
Keywords
Cyanide , ?-Hydroxy nitrile , diHETEs , 5-HETE , 5-oxo-ETE , Thionocarbonates
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1844377
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