A Novel 2’-Deoxynucleoside Designed for Enhanced Recognition of AT Base-pairs. Page 1
Tetrahedron Lerrers, Vol. 37, No. 49, pp. 8857-8860. 1996 Copyright 0 1996 Elsevier …

The N-acetyl derivatives 1a and 2a of the aminotriazole and aminoimidazole 2′-
deoxynucleosides 1 and 2 were synthesized as potential substitutes of protonated 2 …

Oligonucleotides containing 7-bromo-7-deaza-2, 8-diaza-2′-deoxyadenosine () and 5-
amino-3-bromo-4-carbamoyl-1-(2′-deoxy-β-d-erythro-pentofuranosyl) pyrazole () were …

Oligonucleotides containing 2′-deoxyribonucleotides bearing hydroxyphenyl nucleobases
or their 2′, 4′-BNA-modified analogs were synthesized, and the triplex-forming ability of …

Recognition of dsDNA by a triplex-forming oligonucleotide (TFO) is limited to homopurine·
homopyrimidine sequences. Therefore, it is necessary to develop novel nucleoside …

In an effort to construct non-natural bases to be used in triplex-based antigene DNA
recognition strategies, a uriedo-isoindolin-1-one homo-N-nucleoside base was designed to …

2′-Deoxy-N4-phenylcarbamoylcytidine (Pc) was designed for triplex recognition of the
cytosine {guanine base pair at physiological pH values to assist in the development of triplex …

The nucleoside analogues 2′-O-dimethylaminoethoxy uridine and 5-
dimethylaminopropargyl deoxyuridine have been synthesised and incorporated into …

6-(Thiazolyl-5) benzimidazole (B t) was designed as a novel nucleobase for the specific
recognition of an inverted A⊙ T base pair in a triple helix motif. It was successfully …

In this paper, we describe the synthesis of the 3′-3′-linked oligonucleotides connected
with pentaerythritol composed of asymmetrical sequences. Stability of the triplexes between …