FPMP-protected α-hydroxyphosphonate diesters for the synthesis of pro- oligonucleotides

Article abstract of DOI:10.1080/07328319708002933

The synthesis of Fpmp-protected α-hydroxybenzylphosphonate diesters as building blocks for the oligonucleotide synthesis is described. The modified oligonucleotides obtained after cleavage from the solid support and deprotection of the acid-labile Fpmp group should lead to potential pro- oligonucleotides.

Full text of DOI:10.1080/07328319708002933

Nucleosides and Nucleotides
ISSN: 0732-8311 (Print) (Online) Journal homepage: http://www.tandfonline.com/loi/lncn19
Fpmp-Protected α-Hydroxyphosphonate Diesters
for The Synthesis of Pro-Oligonucleotides
Ralf P. Mauritz & Chris Meier
To cite this article: Ralf P. Mauritz & Chris Meier (1997) Fpmp-Protected α-
Hydroxyphosphonate Diesters for The Synthesis of Pro-Oligonucleotides, Nucleosides and
Nucleotides, 16:5-6, 675-678, DOI: 10.1080/07328319708002933
To link to this article: http://dx.doi.org/10.1080/07328319708002933
Published online: 22 Aug 2006.
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Date: 13 June 2016, At: 14:28