Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

A novel thymidine analogue containing both 5-aminopropargyl and 2'-aminoethoxy modifications has been synthesised and incorporated into a triplex-forming oligonucleotide; the combination of the two amino groups on the same nucleoside greatly enhances triplex stability.

Original publication

DOI

10.1039/b006268p

Type

Journal article

Journal

Chemical Communications

Publication Date

07/12/2000

Pages

2315 - 2316