Pilar Ventosa-Andrés

发表

DRUG SOLUBILITY : IMPORTANCE AND ENHANCEMENT TECHNIQUES

Pilar Ventosa-Andrés, Yolanda Fernández Gadea, Yolanda Fernández Gadea, 2016 .

Studies on the reduction and reductive alkylation of amino acid-derived spirocyclic 2,6-dioxopiperazines

M. García-López, J. A. González-Vera, Pilar Ventosa-Andrés, 2007 .

Design, synthesis and biological evaluation of new peptide-based ureas and thioureas as potential antagonists of the thrombin receptor PAR1.

M. García-López, Pilar Ventosa-Andrés, Ángel M. Valdivielso, 2012, European journal of medicinal chemistry.

Peptidomimetics via Iminium Ion Chemistry on Solid Phase: Single, Fused, and Bridged Heterocycles

Agustina La-Venia, Pilar Ventosa-Andrés, V. Krchňák, 2015 .

Highly functionalized 2-oxopiperazine-based peptidomimetics: an approach to PAR1 antagonists.

M. García-López, Pilar Ventosa-Andrés, M. Gutiérrez-Rodríguez, 2013, European journal of medicinal chemistry.

Synthesis and antitumoral evaluation of indole alkaloid analogues containing an hexahydropyrrolo[1',2',3':1,9a,9]imidazo[1,2-a]indole skeleton.

J. A. González-Vera, Pilar Ventosa-Andrés, Ángel M. Valdivielso, 2008, Bioorganic & medicinal chemistry.

A study on the induction of stereoselectivity in the Strecker synthesis of basic amino acid-derived α-amino nitriles

M. García-López, Pilar Ventosa-Andrés, R. Herranz, 2012 .

Chameleonic reactivity of α-amino nitrile-derived ureas. Synthesis of highly functionalized imidazolidin-2-one and imidazolidine-2,4-dione derivatives

M. García-López, J. A. González-Vera, Pilar Ventosa-Andrés, 2014 .

Synthesis and regioselective functionalization of piperazin-2-ones based on Phe-Gly pseudodipeptides

M. García-López, Pilar Ventosa-Andrés, M. Gutiérrez-Rodríguez, 2013 .

Synthesis of Nature-Inspired Medium-Sized Fused Heterocycles from Amino Acids.

Agustina La-Venia, Pilar Ventosa-Andrés, V. Krchňák, 2015, Chemistry.

Solvent-free synthesis of α-amino nitrile-derived ureas.

M. García-López, J. A. González-Vera, Pilar Ventosa-Andrés, 2013, Organic letters.

Solid-phase synthesis of fused 1,4-diazepanone peptidomimetics via tandem N-iminium ion cyclization–nucleophilic addition

Agustina La-Venia, Pilar Ventosa-Andrés, V. Krchňák, 2015 .

Privileged structures as peptide backbone constraints: polymer-supported stereoselective synthesis of benzimidazolinopiperazinone peptides.

Pilar Ventosa-Andrés, V. Krchňák, Ludmila Hradilová, 2014, ACS combinatorial science.

From amino acids to nature-inspired molecular scaffolds: incorporation of medium-sized bridged heterocycles into a peptide backbone.

Agustina La-Venia, Pilar Ventosa-Andrés, V. Krchňák, 2014, The Journal of organic chemistry.