Publicaciones en colaboración con investigadores/as de University of Ferrara (9)

2005

  1. Regioselective one-pot synthesis of 9-alkyl-6-chloropyrido[3,2-e][1,2,4] triazolo-[4,3-a]pyrazines. Reactivity of aliphatic and aromatic hydrazides

    Journal of Organic Chemistry, Vol. 70, Núm. 7, pp. 2878-2880

2004

  1. Synthesis and biological evaluation of novel N6-[4-(substituted) sulfonamidophenylcarbamoyl]adenosine-5′-uronamides as A3 adenosine receptor agonists

    Journal of Medicinal Chemistry, Vol. 47, Núm. 22, pp. 5535-5540

2003

  1. Synthesis and spectral study of a novel distamycin conjugate

    Magnetic Resonance in Chemistry, Vol. 41, Núm. 6, pp. 478-480

2002

  1. An efficient one-pot synthesis of 6-alkoxy-8,9-dialkylpurines via reaction of 5-amino-4-chloro-6-alkylaminopyrimidines with N,N-dimethylalkaneamides and alkoxide ions

    Tetrahedron, Vol. 58, Núm. 38, pp. 7607-7611

  2. Design, synthesis, and biological activity of hybrid compounds between uramustine and DNA minor groove binder distamycin A

    Journal of Medicinal Chemistry, Vol. 45, Núm. 17, pp. 3630-3638

2001

  1. Design, synthesis and biological activity of 5-fluorouracil-distamycin hybrids

    Medicinal Chemistry Research, Vol. 10, Núm. 6, pp. 390-403

1997

  1. Synthesis, chemical solvolytic stability and preliminary biological evaluation of (±)-N-Boc-CPzI: A pyrazole analog of the left-hand segment of the antitumor agent CC-1065

    Anti-Cancer Drug Design, Vol. 12, Núm. 1, pp. 67-74

1996

  1. 1H-Pyrazolo[4,3-d]pyrimidine-7(6H)-one and 5H-Pyrazolo[4,3-d] 1,2,3-triazin-4(3H)-one Derivatives: Synthesis and in vitro biological activity at adenosine A1 and A2a receptors

    Arzneimittel-Forschung/Drug Research, Vol. 46, Núm. 4, pp. 365-368

  2. Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: Potent and selective A2A adenosine antagonists

    Journal of Medicinal Chemistry, Vol. 39, Núm. 5, pp. 1164-1171