I. Collado

发表

Transaminases Applied to the Synthesis of High Added-Value Enantiopure Amines

E. Busto, I. Lavandera, V. Gotor‐Fernández, 2014 .

(2S,1'S,2'S,3'R)-2-(2'-carboxy-3'-methylcyclopropyl) glycine is a potent and selective metabotropic group 2 receptor agonist with anxiolytic properties.

D. Schoepp, C. Pedregal, A. Mazon, 2002, Journal of medicinal chemistry.

Total Synthesis of Spinosyn A. 2. Degradation Studies Involving the Pure Factor and Its Complete Reconstitution

M. Purdie, L. Paquette, I. Collado, 1998 .

Baeyer–Villiger monooxygenase-catalyzed desymmetrizations of cyclobutanones. Application to the synthesis of valuable spirolactones

I. Lavandera, V. Gotor‐Fernández, V. Gotor, 2016 .

Stereocontrolled Synthesis of 5α- and 5β-Substituted Kainic Acids

C. Pedregal, A. Mateo, J. Ezquerra, 1999 .

STEREOSELECTIVE ADDITION OF GRIGNARD-DERIVED ORGANOCOPPER REAGENTS TO N-ACYLIMINIUM IONS : SYNTHESIS OF ENANTIOPURE 5- AND 4,5-SUBSTITUTED PROLINATES

C. Pedregal, J. Ezquerra, I. Collado, 1995 .

Diastereoselective functionalization of 5-hydroxy prolinates by tandem Horner-Emmons-Michael reaction

C. Pedregal, J. J. Vaquero, J. Ezquerra, 1994 .

C3'-cis-Substituted carboxycyclopropyl glycines as metabotropic glutamate 2/3 receptor agonists: synthesis and SAR studies.

D. Schoepp, C. Pedregal, J. Pérez-Castells, 2005, Bioorganic & medicinal chemistry.

Stereoselective Cyclopropanation of Enones with Ethyl Dimethylsulfonium Acetate Bromide in the Presence of DBU.

C. Pedregal, C. Domínguez, J. Monn, 1997 .

2,3'-disubstituted-2-(2'-carboxycyclopropyl)glycines as potent and selective antagonists of metabotropic glutamate receptors.

D. Schoepp, C. Pedregal, A. Mazon, 1998, Bioorganic & medicinal chemistry letters.

Stereoselective cyclopropanation of enones with ethyl dimethylsulfonium acetate bromide in the presence of DBU

C. Pedregal, C. Domínguez, J. Monn, 1997 .

Dipeptides as effective prodrugs of the unnatural amino acid (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740), a selective group II metabotropic glutamate receptor agonist.

M. Clay, T. Lindstrom, D. Schoepp, 2005, Journal of medicinal chemistry.

First Trapping Reaction of N-Boc Ethyl 3,4-Dehydropyroglutamate with Cyclopentadiene

C. Pedregal, J. Ezquerra, A. Rubio, 1995 .

4-Alkyl- and 4-cinnamylglutamic acid analogues are potent GluR5 kainate receptor agonists.

B. Ballyk, C. Dominguez, D. Bleakman, 2000, Journal of medicinal chemistry.

Privileged structure based ligands for melanocortin receptors--substituted benzylic piperazine derivatives.

P. Ornstein, K. Briner, M. J. Fisher, 2005, Bioorganic & medicinal chemistry letters.

(2S,1'S,2'R,3'R)-2-(2'-Carboxy-3'-hydroxymethylcyclopropyl) glycine is a highly potent group 2 and 3 metabotropic glutamate receptor agonist with oral activity.

D. Schoepp, C. Pedregal, J. Pérez-Castells, 2004, Journal of medicinal chemistry.

4-Alkylidenyl glutamic acids, potent and selective GluR5 agonists.

B. Ballyk, C. Dominguez, D. Bleakman, 2000, Bioorganic & medicinal chemistry letters.

Privileged structure based ligands for melanocortin-4 receptors--aliphatic piperazine derivatives.

P. Ornstein, K. Briner, M. J. Fisher, 2006, Bioorganic & medicinal chemistry letters.

(2S,1'S,2'R,3'R)-2(2'-Carboxy-3'-hydroxymethylcyclopropyl)glycine-[3H], a potent and selective radioligand for labeling group 2 and 3 metabotropic glutamate receptors.

D. Schoepp, C. Pedregal, P. Kulanthaivel, 2005, Bioorganic & medicinal chemistry letters.