A simple and efficient procedure for the synthesis of 5'-aminoalkyl oligodeoxynucleotides.

Abstract:

:Synthetic deoxyoligonucleotides have been 5'-aminoalkylated at the end of step-wise synthesis on the polymer support. This was achieved through the activation of the 5'-hydroxyl group as its 5'-imidazolyl derivative using carbonyldiimidazole, which was subsequently displaced with hexamethylene diamine to yield the title compound. The alkyl carbamate linkage thus generated withstands the deprotection conditions used in oligonucleotide synthesis. Purification by gel electrophoresis and further derivatization at the 5'-amino group with N-hydroxysuccinimidobiotin is described.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Wachter L,Jablonski JA,Ramachandran KL

doi

10.1093/nar/14.20.7985

subject

Has Abstract

pub_date

1986-10-24 00:00:00

pages

7985-94

issue

20

eissn

0305-1048

issn

1362-4962

journal_volume

14

pub_type

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