Additions of Thiols to 7-Vinyl-7-deazaadenine Nucleosides and Nucleotides. Synthesis of Hydrophobic Derivatives of 2′-Deoxyadenosine, dATP and DNA-Reference-Cited by-同舟云学术

Additions of Thiols to 7-Vinyl-7-deazaadenine Nucleosides and Nucleotides. Synthesis of Hydrophobic Derivatives of 2′-Deoxyadenosine, dATP and DNA

Published:2016-10-14 Issue:22 Volume:81 Page:11115-11125
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Slavíčková Michaela¹,Pohl Radek¹,Hocek Michal¹²

Affiliation:

1. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Gilead & IOCB Research Center, Flemingovo namesti 2, CZ-16610 Prague 6, Czech Republic

2. Department of Organic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, Prague-2 12843, Czech Republic

Funder

Grantová Agentura Ceské Republiky

Akademie Ved Ceské Republiky

Gilead Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02098

Reference53 articles.

1. Nucleoside, nucleotide and oligonucleotide based amphiphiles: a successful marriage of nucleic acids with lipids

2. Hybrid lipid oligonucleotide conjugates: synthesis, self-assemblies and biomedical applications

3. Lipophilic nucleic acids — A flexible construction kit for organization and functionalization of surfaces

4. DNA-Based Micelles: Synthesis, Micellar Properties and Size-Dependent Cell Permeability

5. Application of nucleic acid–lipid conjugates for the programmable organisation of liposomal modules

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