Title of article :
Practical syntheses of 4-fluoroprolines
Author/Authors :
Chorghade، نويسنده , , Mukund S. and Mohapatra، نويسنده , , Debendra K. and Sahoo، نويسنده , , Gokarneswar and Gurjar، نويسنده , , Mukund K. and Mandlecha، نويسنده , , Manish V. and Bhoite، نويسنده , , Nitin and Moghe، نويسنده , , Santosh and Raines، نويسنده , , Ronald T.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
4
From page :
781
To page :
784
Abstract :
4-Fluoroprolines are among the most useful nonnatural amino acids in chemical biology. Here, practical routes are reported for the synthesis of the 2S,4R, 2S,4S, and 2R,4S diastereomers of 4-fluoroproline. Each route starts with (2S,4R)-4-hydroxyproline, which is a prevalent component of collagen and hence readily available, and uses a fluoride salt to install the fluoro group. Hence, the routes provide process-scale access to these useful nonnatural amino acids.
Keywords :
4-Fluoroproline , nonnatural amino acid , Collagen , Process-scale synthesis , 4-Hydroxyproline
Journal title :
Journal of Fluorine Chemistry
Serial Year :
2008
Journal title :
Journal of Fluorine Chemistry
Record number :
1610206
Link To Document :
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