Synlett 2024; 35(06): 711-715
DOI: 10.1055/a-2071-7168
cluster
Special Issue to Celebrate the Centenary Year of Prof. Har Gobind Khorana

Acyclic 2-Ethynylnaphthalene-Modified 8-Aza-3,7-dideaza-2′-deoxyadenosine Allows Thymine Discrimination by Probing the DNA Minor Groove Environment

Yurino Oku
,
Misaki Kai
,
Saika Kobayashi
,
Ryuzi Katoh
,
Yoshio Saito
This work was supported by the Japan Society for the Promotion of Science (MEXT, KAKENHI) (Grant No. 19K05700).


Abstract

Two novel acyclic environment-sensitive fluorescent nucleosides named ac37zA and an37zA are synthesized and their photophysical properties are investigated. Both ac37zA and an37zA exhibit dual fluorescence emission depending upon molecular coplanarity. Oligodeoxynucleotide probes containing ac37zA clearly discriminate perfectly matched thymine in target DNA strands by strong charge transfer (CT) emission in the longer wavelength region and by strong quenching of emission from the twisted conformation in the mismatched case.

Supporting Information



Publikationsverlauf

Eingereicht: 14. Februar 2023

Angenommen nach Revision: 11. April 2023

Accepted Manuscript online:
11. April 2023

Artikel online veröffentlicht:
23. Mai 2023

© 2023. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References and Notes

  • 7 Synthesis of 1 A mixture of 8 (36.1 mg, 0.10 mmol), Pd(PPh3)4 (46.2 mg, 4.0 × 10–2 mmol), CuI (7.6 mg, 4.0 × 10–2 mmol) and 2-naphthonitrile (24.7 mg, 0.14 mmol) in dry DMF (1.35 mL) and Et3N (0.36 mL) was stirred at 60 °C under an argon atmosphere for 1 h. After cooling to room temperature, the reaction mixture was concentrated in vacuo. The residue was purified by silica gel column chromatography, eluting with CHCl3/MeOH (15:1 to 5:1), to give 1 (25.1 mg, 61%) as a pale yellow solid. 1H NMR (400 MHz, DMSO-d 6): δ = 1.55 (m, 2 H), 1.91 (m, 1 H), 2.05 (m, 1 H), 3.45 (m, 2 H), 3.72 (m, 1 H), 4.37 (t, J = 4.4, 9.6 Hz, 1 H), 4.70–4.78 (complex, 2 H), 4.90 (m, 1 H), 7.37 (br s, 2 H), 7.82 (m, 2 H), 8.03 (s, 1 H), 8.09 (t, J = 9.2, 17.6 Hz, 2 H), 8.26 (s, 1 H), 8.30 (s, 1 H), 8.60 (s, 1 H). 13C NMR (100 MHz, DMSO-d 6): δ = 38.4, 46.9, 57.8, 65.2, 69.8, 88.1, 90.3, 92.8, 107.3, 108.8, 119.2, 123.8, 127.2, 129.0, 129.1, 129.4, 129.9, 131.0, 133.3, 134.1, 134.2, 140.9, 150.0, 154.6. HRMS (ESI): m/z [M + Na]+ calcd for C24H21N5O2Na: 434.1593; found: 434.1618.
  • 8 Morris JV, Mahaney MA, Huber JR. J. Phys. Chem. 1976; 80: 969