Home / Publications / Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling

Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling

0
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Wang S. et al. Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling // Mendeleev Communications. 2019. Vol. 29. No. 5. pp. 503-505.
GOST all authors (up to 50) Copy
Wang S., Liu F., Fang J., Li Y., Liu J., Liu M. Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling // Mendeleev Communications. 2019. Vol. 29. No. 5. pp. 503-505.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2019.09.008
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.008
TI - Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling
T2 - Mendeleev Communications
AU - Wang, Shiyu
AU - Liu, Feifan
AU - Fang, Jiaobing
AU - Li, Yashu
AU - Liu, Jun
AU - Liu, Mingzhe
PY - 2019
DA - 2019/09/04
PB - Mendeleev Communications
SP - 503-505
IS - 5
VL - 29
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Wang,
author = {Shiyu Wang and Feifan Liu and Jiaobing Fang and Yashu Li and Jun Liu and Mingzhe Liu},
title = {Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.008},
number = {5},
pages = {503--505},
doi = {10.1016/j.mencom.2019.09.008}
}
MLA
Cite this
MLA Copy
Wang, Shiyu, et al. “Synthesis of a new alkynylated deoxyadenosine phosphoramidite for the click reaction-mediated DNA labeling.” Mendeleev Communications, vol. 29, no. 5, Sep. 2019, pp. 503-505. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.008.

Abstract

A new 5′-dimethoxytrityl N6-alkynylated 2′-deoxyadenosine phosphoramidite has been designed and synthesized from 2′-deoxyadenosine. The applicability of this building block for the production of alkyne-modified oligodeoxynucleotide has been demonstrated. This allows one to introduce various labels into DNA using the click reaction.

References

1.
From Mechanism to Mouse: A Tale of Two Bioorthogonal Reactions
Sletten E.M., Bertozzi C.R.
Accounts of Chemical Research, 2011
3.
Benz-in als Dipolarophil
Huisgen R., Knorr R.
Die Naturwissenschaften, 1961
5.
Click Chemistry: Diverse Chemical Function from a Few Good Reactions
Kolb H.C., Finn M.G., Sharpless K.B.
Angewandte Chemie - International Edition, 2001
9.
Click chemistry with DNA
El-Sagheer A.H., Brown T.
Chemical Society Reviews, 2010
10.
Click–Click–Click: Single to Triple Modification of DNA
Gramlich P. ., Warncke S., Gierlich J., Carell T.
Angewandte Chemie - International Edition, 2008
11.
Click Chemistry as a Reliable Method for the High-Density Postsynthetic Functionalization of Alkyne-Modified DNA
Gierlich J., Burley G.A., Gramlich P.M., Hammond D.M., Carell T.
Organic Letters, 2006
14.
Comparison of a Nucleosidic vs Non-Nucleosidic Postsynthetic “Click” Modification of DNA with Base-Labile Fluorescent Probes
Berndl S., Herzig N., Kele P., Lachmann D., Li X., Wolfbeis O.S., Wagenknecht H.
Bioconjugate Chemistry, 2009
15.
New Strategies for Cyclization and Bicyclization of Oligonucleotides by Click Chemistry Assisted by Microwaves
16.
Simple SNP typing assay using a base-discriminating fluorescent probe
Okamoto A., Tainaka K., Ochi Y., Kanatani K., Saito I.
Molecular BioSystems, 2006
20.
An Overview of Some Recent Developments in Ionization Methods for Mass Spectrometry
22.
Amide bond formation and peptide coupling
Montalbetti C.A., Falque V.
Tetrahedron, 2005
23.
Self-Duplex Formation of an APy-Substituted Oligodeoxyadenylate and Its Unique Fluorescence
Seo Y.J., Rhee H., Joo T., Kim B.H.
Journal of the American Chemical Society, 2007