Alessandra Cordeiro

Selective inhibition of human inmunodeficiency virus type 1 ( HIV-1 ) by nucleoside analogues with an unusual tricyclic structure

J. Balzarini, M. Camarasa, E. Quesada, 2014 .

Selective inhibition of Human Immunodeficiency Virus type 1 (HIV-1) by a novel family of tricyclic nucleosides.

E. Vanstreels, J. Balzarini, M. Camarasa, 2011, Antiviral research.

Synthesis of 6‐Nitro‐1,2,3,4‐tetrahydroquinoline: An Experimental and Theoretical Study of Regioselective Nitration

J. O'Brien, I. Rozas, F. Blanco, 2011 .

New bladed habit of hexadecanoic-acid crystals observed by SEM combined with XRD, FT-IR and Raman studies

P. Freire, S. Morelhão, G. Saraiva, 2020 .

Novel [2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]- 3'-spiro-5''-(4''-amino-1'',2''-oxathiole-2'',2" -dioxide) derivatives with anti-HIV-1 and anti-human-cytomegalovirus activity.

E. De Clercq, J. Balzarini, M. Camarasa, 2005, Journal of medicinal chemistry.

Synthesis of novel Bi-, Tri-, and tetracyclic nucleosides by reaction of a common cyclic enamine derived from TSAO-T with nucleophiles.

M. Camarasa, M. Jimeno, C. Chamorro, 2004, The Journal of organic chemistry.

Towards more specific O6-methylguanine-DNA methyltransferase (MGMT) inactivators.

G. Margison, I. Rozas, T. McMurry, 2011, Bioorganic & medicinal chemistry.