Search Results - "Spadafora, Marie"

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

Authors: Spadafora, Marie Mehiri, Mohamed Burger, Alain et al.

Source: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Jun2008, Vol. 49 Issue 25, p3967-3971. 5p.

Subjects: Acid-base chemistry, Physical & theoretical chemistry, Acid neutralizing capacity, Lewis acids

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

Authors: Dziuba, Dmytro Postupalenko, Viktoriia Y. Spadafora, Marie et al.

Source: Journal of the American Chemical Society; 6/20/2012, Vol. 134 Issue 24, p10209-10213, 5p

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

Authors: Kaloudis, Panagiotis D'Angelantonio, Mila Guerra, Maurizio et al.

Source: Journal of the American Chemical Society; 11/4/2009, Vol. 131 Issue 43, p15895-15902, 8p

Efficient Synthesis of Ratiometric Fluorescent Nucleosides Featuring 3-Hydroxychromone Nucleobases

Authors: Spadafora, Marie Postupalenko, Victoria Y. Shvadchak, Volodymyr V. et al.

Source: Tetrahedron. Sep2009, Vol. 65 Issue 37, p7809-7816. 8p.

Efficient Synthesis of α- and β-2′-Deoxy-heteroaryl-C-nucleosides.

Authors: Spadafora, Marie Burger, Alain Benhida, Rachid

Source: Synlett. 2008, Issue 8, p1225-1229. 5p.

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

Authors: Kaloudis, Panagiotis D'Angelantonio, Mila Guerra, Maurizio et al.

Source: Journal of the American Chemical Society. 11/4/2009, Vol. 131 Issue 43, p15895-15902. 8p.