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Literature DB >> 23090440

A ferrocene nucleic acid oligomer as an organometallic structural mimic of DNA.

Huy V Nguyen¹, Zheng-yun Zhao, Antoine Sallustrau, Sarah L Horswell, Louise Male, Andrea Mulas, James H R Tucker.

Abstract

The design, synthesis and electrochemical behaviour of an oligomer consisting of linked thymine-functionalised ferrocene units are reported, which, as a so-called form of ferrocene nucleic acid (FcNA), acts as a structural mimic of DNA.

Entities: Chemical

Mesh：

Substances：

Year: 2012 PMID： 23090440 DOI： 10.1039/c2cc36428j

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

7 in total

1. Artificial Sandwich Base for Monitoring Single-Nucleobase Changes and Charge-Transfer Rates in DNA.

Authors: Razack Abdullah; Sitao Xie; Ruowen Wang; Cheng Jin; Yulin Du; Ting Fu; Juan Li; Jie Tan; Lili Zhang; Weihong Tan
Journal: Anal Chem Date: 2019-01-08 Impact factor: 6.986

2. Mix and match backbones for the formation of H-bonded duplexes.

Authors: Giulia Iadevaia; Alexander E Stross; Anja Neumann; Christopher A Hunter
Journal: Chem Sci Date: 2016-01-07 Impact factor: 9.825

3. Homochiral oligomers with highly flexible backbones form stable H-bonded duplexes.

Authors: Diego Núñez-Villanueva; Christopher A Hunter
Journal: Chem Sci Date: 2016-08-19 Impact factor: 9.825

4. Backbone conformation affects duplex initiation and duplex propagation in hybridisation of synthetic H-bonding oligomers.

Authors: Giulia Iadevaia; Diego Núñez-Villanueva; Alexander E Stross; Christopher A Hunter
Journal: Org Biomol Chem Date: 2018-06-06 Impact factor: 3.876

A ferrocene nucleic acid oligomer as an organometallic structural mimic of DNA.

1. Artificial Sandwich Base for Monitoring Single-Nucleobase Changes and Charge-Transfer Rates in DNA.

2. Mix and match backbones for the formation of H-bonded duplexes.

3. Homochiral oligomers with highly flexible backbones form stable H-bonded duplexes.

4. Backbone conformation affects duplex initiation and duplex propagation in hybridisation of synthetic H-bonding oligomers.

5. H-Bonded Duplexes based on a Phenylacetylene Backbone.

6. Cooperative duplex formation by synthetic H-bonding oligomers.

7. Sequence-Selective Formation of Synthetic H-Bonded Duplexes.