Solid-phase synthesis of oligodeoxynucleotides containing O6-alkylguanine.

Abstract:

:Practical methods for the routine solid-phase synthesis of oligodeoxynucleotides containing O6-alkylguanine are described. It is shown that if the 2-amino group of the alkylated base is protected with a phenylacetyl group, and a mixture of nitrobenzaldoximate ions and ammonia used to remove the protecting groups from the oligomer at the end of the synthesis, there is negligible formation of 2,6-diaminopurine and that after chromatography pure oligomers are obtained.

journal_name

Carcinogenesis

journal_title

Carcinogenesis

authors

Smith CA,Xu YZ,Swann PF

doi

10.1093/carcin/11.5.811

subject

Has Abstract

pub_date

1990-05-01 00:00:00

pages

811-6

issue

5

eissn

0143-3334

issn

1460-2180

journal_volume

11

pub_type

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