M. Beier et W. Pfleiderer, Nucleotides - Part LXI - Phthaloyl strategy: A new concept of oligonucleotide synthesis, HELV CHIM A, 82(4), 1999, pp. 633-644
A new alternative strategy of oligonucleotide synthesis was developed by us
e of thr phthaloyl protecting group for the exocyclic amino functions of th
e nucleobases (see 9 - 12). This approach combines the advantages of cheap
and easily accessable monomeric building blocks (see 17 - 20), standard mac
hine-aided oligonucleotide synthesis, and a fast deprotection protocol whic
h is orthogonal to the cleavage procedure from the solid support. The crude
oligonucleotides show high purity and require, in general, no further chro
matographic purification.