C. Peña

Conformationally Biased Selective Alkylation of trans-Cyclohexane-1,2-bis(sulfonamide) Assisted by Solvent-Tuned Protecting Groups: Applications to the Synthesis of a Large Optically Active Polyazamacrocycle†

I. Alfonso, V. Gotor, C. Peña, 2006 .

An improved chemoenzymatic synthesis of both enantiomers of trans-cyclopentane-1,2-diamine

V. Gotor, Javier González‐Sabín, F. Rebolledo, 2008 .

Cycloalkane-1,2-diamine derivatives as chiral solvating agents. Study of the structural variables controlling the NMR enantiodiscrimination of chiral carboxylic acids

I. Alfonso, V. Gotor, Javier González‐Sabín, 2008 .

New pincer-like receptor derived from trans-cyclopentane-1,2-diamine as a chiral shift reagent for carboxylic acids

I. Alfonso, V. Gotor, Javier González‐Sabín, 2007 .

Solvent dependent selective alkylation of a bis(sulfonamide) for the synthesis of a DNA-binding chiral polyamine

N. Voelcker, I. Alfonso, V. Gotor, 2005 .

Synthesis and stereoselective DNA binding abilities of new optically active open-chain polyamines.

N. Voelcker, I. Alfonso, V. Gotor, 2007, The Journal of organic chemistry.

Highly efficient chemoenzymatic syntheses of trans-2-aminocyclopentanol derivatives

F. Morís-Varas, V. Gotor, Javier González‐Sabín, 2009 .