Current Organic Chemistry

Author(s): Vadim D. Romanenko and Valery P. Kukhar

DOI: 10.2174/138527281811140815124708

Progress in the Development of Pyrophosphate Bioisosteres: Synthesis and Biomedical Potential of 1-Fluoro- and 1,1-Difluoromethylene-1,1-bisphosphonates

Page: [1491 - 1512] Pages: 22

  • * (Excluding Mailing and Handling)

Abstract

Mono- and difluoromethylenebisphosphonates are of great synthetic and biological interest since they are among the best isopolar pyrophosphate mimics. This review will emphasize preparation and some of the most important applications of these compounds. The following synthetic approaches to fluoromethylenebisphosphonates are summarized: (i) electrophilic halogenation, (ii) Arbuzov and Michaelis-Becker reactions, (iii) direct electrophilic phosphorylation of fluoromethylphosphonate carbanions, and (iv) autocondensation of fluoromethylphosphonate carbanions. Emphasis is given to the synthesis and biomedical application of modified nucleoside polyphosphates, incorporating fluoromethylenebisphosphonate scaffold.

Keywords: Enzyme inhibitors, fluorinated bisphosphonates, modified nucleoside polyphosphates, phosphate mimics, synthetic methods

Graphical Abstract