4.8 Article

Orthogonal Synthesis of Easy-to-Read Information-Containing Polymers Using Phosphoramidite and Radical Coupling Steps

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 138, Issue 30, Pages 9417-9420

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b06222

Keywords

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Funding

  1. European Union [642083]
  2. IDEX program of the University of Strasbourg
  3. CNRS
  4. ITN Euro-Sequences
  5. IDEX program
  6. Marie Curie Actions (MSCA) [642083] Funding Source: Marie Curie Actions (MSCA)

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A new orthogonal solid-phase iterative strategy is proposed for the synthesis of sequence-coded polymers. This approach relies on the use of two successive chemoselective steps: (i) phosphoramidite coupling, and (ii) radical radical coupling. These repeated steps can be performed using two different types of building blocks, i.e. a phosphoramidite monomer that also contains an alkyl bromide and a hydroxy-functionalized nitroxide. The phosphoramidite and the hydroxy group are reacted in step (i), thus leading to a phosphite that is oxidized in situ into a phosphate bond. The alkyl bromide is activated by copper bromide in step (ii) to afford a carbon-centered radical that is spin-trapped in situ by the nitroxide. The iterative repetition of these steps allow synthesis of uniform polymers, as evidenced by high resolution electrospray mass spectrometry. Moreover, binary information could be easily implemented in the polymers using different types of phosphoramidite monomers in step (i). Interestingly, it was found that the formed information-containing polymers are very easy to sequence by tandem mass spectrometry due to the presence of easily cleavable alkoxyamine bonds formed in step (ii).

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