Literature DB >> 3654813

Polymer support synthesis. XII. Derivatization with the 4-decyloxytrityl group as an aid in the affinity chromatography of oligo- and polynucleotides.

H Seliger1, G Schmidt.   

Abstract

In a continuation of previous studies on trityl groups substituted with long alkyl chains as affinity-protecting groups for oligonucleotides, the use of the (4-decyloxyphenyl)diphenylmethyl (DTr) group as an aid in the separation of solid-phase products has been investigated. This substituent, which can be introduced and removed from the 5'-position in a similar manner to the di-p-anisylphenylmethyl group, helps in the purification of deoxypolynucleotides with up to 140 bases. Their retention time was shown to depend not only on the length of the nucleotide chain and alkyl substituent, but also on the elution gradient rate. In oligoribonucleotide synthesis, the DTr group allows the purification of partially protected sequences, which are more stable to enzymatic degradation and, therefore, more suitable for handling and storage.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3654813     DOI: 10.1016/s0021-9673(01)84997-9

Source DB:  PubMed          Journal:  J Chromatogr


  2 in total

1.  Improvement in the synthesis of oligonucleotides of extended length by modification of detritylation step.

Authors:  I Habus; S Agrawal
Journal:  Nucleic Acids Res       Date:  1994-10-11       Impact factor: 16.971

2.  Synthesis, hybridization properties and antiviral activity of lipid-oligodeoxynucleotide conjugates.

Authors:  R G Shea; J C Marsters; N Bischofberger
Journal:  Nucleic Acids Res       Date:  1990-07-11       Impact factor: 16.971

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.