M. Spadafora

A universal nucleoside with strong two-band switchable fluorescence and sensitivity to the environment for investigating DNA interactions.

Y. Mély, A. Klymchenko, V. Postupalenko, 2012, Journal of the American Chemical Society.

Comparison of isoelectronic 8-HO-G and 8-NH2-G derivatives in redox processes.

C. Chatgilialoglu, M. Spadafora, Q. G. Mulazzani, 2009, Journal of the American Chemical Society.

Efficient synthesis of ratiometric fluorescent nucleosides featuring 3-hydroxychromone nucleobases.

Y. Mély, A. Klymchenko, V. Shvadchak, 2009 .

Development of environmentally sensitive fluorescent and dual emissive deoxyuridine analogues

Benoît Y. Michel, Y. Mély, A. Demchenko, 2015 .

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

A. Burger, R. Benhida, M. Mehiri, 2008 .