A new modified cytosine base capable of base pairing with guanine using four hydrogen bonds-Reference-Cited by-同舟云学术

A new modified cytosine base capable of base pairing with guanine using four hydrogen bonds

Published:2014 Issue:14 Volume:12 Page:2255-2262
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yamada Ken¹²³,Masaki Yoshiaki¹²³,Tsunoda Hirosuke¹²³,Ohkubo Akihiro¹²³,Seio Kohji¹²³,Sekine Mitsuo¹²³

Affiliation:

1. Department of Life Science

2. Tokyo Institute of Technology

3. Yokohama, 226-8501 Japan

Abstract

Oligonucleotides, containing 4-N-(1H-pyrrol-2-ylcarbonyl)deoxycytidine (dC^Pyc) and related derivatives, were synthesized via deprotection using 1.5 M NaOMe/MeOH.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C3OB42420K

Reference34 articles.

1. Tricyclic 2'-Deoxycytidine Analogs: Syntheses and Incorporation into Oligodeoxynucleotides Which Have Enhanced Binding to Complementary RNA

2. A Cytosine Analogue Capable of Clamp-Like Binding to a Guanine in Helical Nucleic Acids

3. Direct Observation of a Cytosine Analogue that Forms Five Hydrogen Bonds to Guanosine: Guanidino G-Clamp

4. Specific Fluorescent Probe for 8-Oxoguanosine

5. A Highly Fluorescent DNA Base Analogue that Forms Watson−Crick Base Pairs with Guanine

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