Journal
JOURNAL OF FLUORINE CHEMISTRY
Volume 112, Issue 1, Pages 13-33Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/S0022-1139(01)00478-X
Keywords
(alpha-monofluoroalkyl)phosphonate; phosphate mimics; triflate displacement; glucose 6-phosphate dehydrogenase; glycerol 3-phosphate dehydrogenase; protein phosphotyrosine phosphatase PTP1B
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In the early 1980s, Blackburn and McKenna suggested that a-fluorination might lead to phosphonates that better mimic natural phosphates. Although alpha -monofluorination produces phosphonates with matching second pK(a) values, the alpha,alpha -difluorinated phosphonates have received more attention in the past decade or so. Recently, reported enzyme kinetic data on the a-monofluorinated phosphonates from the O'Hagan lab and from our lab suggest that the CHF stereochemistry does affect enzyme-binding, thereby providing an additional variable that may be tuned to achieve optimal binding to an active site of interest. This asymmetry also appears in structural data from the groups of Barford/Burke and Tracey on PTP1B complexes with bound a,a-difluorinated phosphonate inhibitors. In those complexes, only one of two prochiral fluorine atoms appears to interact appreciably with the enzyme. Namely, it is thought that the pro-R (F-si) fluorine is engaged in an important hydrogen bond with the Phe-182 amide NH. Available methods for the synthesis of this class of alpha -monofluorinated phosphonates are reviewed. A new convergent approach, developed at Nebraska, in which the potassium anion of (alpha -fluoro-alpha -phenylsulfonylmethyl)phosphonate is used to displace primary triflates is also described. This method is particularly convenient as it allows one to perform a fluorinated phosphonate scan of an active site of interest (in what follows, we use this expression to designate the synthesis and evaluation of a complete set of the CH2-, CF2- and both stereoisomeric CHF-phosphonates in an active site of interest) from a single primary triflate. The properties of the title compounds in enzyme active sites are discussed, as are possible interactions of these fluorine-containing bioisosteres with active site residues. (C) 2001 Elsevier Science B.V. All rights reserved.
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