Nucleotides - Part LXI - Phthaloyl strategy: A new concept of oligonucleotide synthesis

Citation
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
Citations number
31
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
HELVETICA CHIMICA ACTA
ISSN journal
0018019X → ACNP
Volume
82
Issue
4
Year of publication
1999
Pages
633 - 644
Database
ISI
SICI code
0018-019X(1999)82:4<633:N-PL-P>2.0.ZU;2-I
Abstract
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.