| Literature DB >> 19727323 |
Mukund S Chorghade1, Debendra K Mohapatra, Gokarneswar Sahoo, Mukund K Gurjar, Manish V Mandlecha, Nitin Bhoite, Santosh Moghe, Ronald T Raines.
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.Entities:
Year: 2008 PMID: 19727323 PMCID: PMC2598397 DOI: 10.1016/j.jfluchem.2008.06.024
Source DB: PubMed Journal: J Fluor Chem ISSN: 0022-1139 Impact factor: 2.050