Detalhe da pesquisa
1.
Synthesis of fluorescent 5-heteroarylpyrimidine-containing oligonucleotides via post-synthetic trifluoromethyl conversion.
Org Biomol Chem
; 22(17): 3510-3517, 2024 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38619422
2.
Photoisomerization of "Partially Embedded Dihydropyridazine" with a Helical Structure.
Chemistry
; 29(62): e202302413, 2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612241
3.
Photoisomerization of "Partially Embedded Dihydropyridazine" with a Helical Structure.
Chemistry
; 29(62): e202303311, 2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37873888
4.
Expansion of Phosphoramidite Chemistry in Solid-Phase Oligonucleotide Synthesis: Rapid 3'-Dephosphorylation and Strand Cleavage.
J Org Chem
; 88(5): 2726-2734, 2023 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36812161
5.
Synthesis of purine derivatives of Me-TaNA and properties of Me-TaNA-modified oligonucleotides.
Org Biomol Chem
; 21(25): 5203-5213, 2023 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37309204
6.
Synthesis and Properties of Oligonucleotides Containing 2'-O,4'-C-Methyleneoxy-Bridged Pyrimidine Derivatives.
J Org Chem
; 87(17): 11743-11750, 2022 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35960869
7.
Artificial Host Molecules to Covalently Capture 8-Nitro-cGMP in Neutral Aqueous Solutions and in Cells.
Bioconjug Chem
; 32(2): 385-393, 2021 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33529519
8.
Push-Pull Bisnaphthyridylamine Supramolecular Nanoparticles: Polarity-Induced Aggregation and Crystallization-Induced Emission Enhancement and Fluorescence Resonance Energy Transfer.
Chemistry
; 27(9): 3039-3046, 2021 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32935395
9.
Characterization and Water-Proton Longitudinal Relaxivities of Liposome-Type Radical Nanoparticles Prepared via a Supramolecular Approach.
Langmuir
; 36(19): 5280-5286, 2020 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32321252
10.
Characterization of Push-Pull-Type Benzo[X]quinoline Derivatives (X = g or f): Environmentally Responsive Fluorescent Dyes with Multiple Functions.
J Org Chem
; 85(20): 13177-13190, 2020 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32940474
11.
A fully synthetic 6-aza-artemisinin bearing an amphiphilic chain generates aggregates and exhibits anti-cancer activities.
Org Biomol Chem
; 18(28): 5339-5343, 2020 07 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32618320
12.
Fluorescence Properties and Exciplex Formation of Emissive Naphthyridine Derivatives: Application as Sensors for Amines.
Chemistry
; 25(65): 14943-14952, 2019 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31512286
13.
Development of Turn-On Probes for Acids Triggered by Aromaticity Enhancement Using Tricyclic Amidine Derivatives.
J Org Chem
; 84(11): 6612-6622, 2019 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31094191
14.
Luminescent europium sensors for specific detection of 8-oxo-dGTP by time-gated fluorescence.
Bioorg Med Chem
; 26(12): 3254-3260, 2018 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29731311
15.
Synthetic receptor molecules for selective fluorescence detection of 8-oxo-dGTP in aqueous media.
Org Biomol Chem
; 14(33): 7949-55, 2016 Aug 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-27488938
16.
New NitroG-Grasp Molecules with Enhanced Capture Reactivity for 8-Nitroguanosine in the Aqueous Media.
Chem Pharm Bull (Tokyo)
; 63(11): 913-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26521855
17.
Development of new 1,3-diazaphenoxazine derivatives (thioG-grasp) to covalently capture 8-thioguanosine.
Molecules
; 20(1): 1078-87, 2015 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25584836
18.
Synthesis of a Hydrophobic Phenanthrene-Containing Universal Support for Solid-Phase Oligonucleotide Synthesis.
Curr Protoc
; 4(3): e1013, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38483118
19.
Generation of 4'-Carbon Radicals via 1,5-Hydrogen Atom Transfer for the Synthesis of Bridged Nucleosides.
Org Lett
; 24(41): 7696-7700, 2022 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36214750
20.
Photophysical Properties of Emissive Pyrido[3,2-c]carbazole Derivatives and Apoptosis Induction: Development towards Theranostic Agents in Response to Light Stimulus.
Chem Asian J
; 14(21): 3938-3945, 2019 Nov 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31560150