Marie Spadafora

A Universal Nucleoside with Strong Two-Band Switchable Fluorescence and Sensitivity to the Environment for Investigating DNA Interactions

Dmytro Dziuba, Viktoriia Postupalenko, Marie Spadafora et al. · Journal of the American Chemical Society · 2012 · 91 citations

Dna Nanotechnology, Biochemistry, Dna Base Stacking +13

Efficient Synthesis of Ratiometric Fluorescent Nucleosides Featuring 3-Hydroxychromone Nucleobases

Marie Spadafora, Victoria Y. Postupalenko, Volodymyr V. Shvadchak et al. · Tetrahedron · 2009 · 67 citations

Bioorganic Chemistry, Oligonucleotide, Efficient Synthesis +2

Development of environmentally sensitive fluorescent and dual emissive deoxyuridine analogues

Nicolas Barthès, Julie Karpenko, Dmytro Dziuba et al. · RSC Advances · 2015 · 38 citations

Engineering, Dna Analysis, Green Chemistry +19

Friedel–Crafts and modified Vorbrüggen ribosylation. A short synthesis of aryl and heteroaryl-C-nucleosides

Marie Spadafora, Mohamed Mehiri, Alain Burger et al. · Tetrahedron Letters · 2008 · 26 citations

Combinatorial Chemistry, Engineering, Biochemistry +7

Comparison of Isoelectronic 8-HO-G and 8-NH₂-G Derivatives in Redox Processes

Panagiotis Kaloudis, Mila D’Angelantonio, Maurizio Guerra et al. · Journal of the American Chemical Society · 2009 · 12 citations

Bioorganic Chemistry, Dna Damage, Engineering +19