A. Rubio

发表

Stereoselective reactions of lithium enolates derived from N-BOC protected pyroglutamic esters

C. Pedregal, F. Sánchez-Ferrando, J. Ezquerra, 1993 .

Stereoselective double alkylation of ethyl N-boc-pyroglutamate

J. Vaquero, C. Pedregal, J. Deeter, 1994 .

4-Substituted D-glutamic acid analogues: the first potent inhibitors of glutamate racemase (MurI) enzyme with antibacterial activity.

Jose-Alfredo Martin, J. Mcgee, Ana Sánchez, 2002, Journal of medicinal chemistry.

A Stereoselective synthesis of conjugated trans trienes: Low-valent titanium induced reductive elimination of 1,6-dibenzoate-2,-dienes

G. Solladié, A. Rubio, G. B. Stone, 1993 .

General method for the synthesis of 5-arylpyrrole-2-carboxylic acids

C. Pedregal, J. Alvarez-Builla, J. J. Vaquero, 1993 .

Stereoselective reductions of 2-keto sulfoxides with hydrides

C. Pedregal, G. Solladié, M. C. Carreño, 1990 .

New enantioselective approach to α-allokainoids by Michael addition to chiral 4-substituted 2,3-didehydroprolinate

A. Escribano, J. Ezquerra, A. Rubio, 1995 .

4-benzyl-2,3-didehydroprolinate as a homochiral template for michael additions. Synthesis of enantiopure α-allokainoids, β-kainoids, 2,3-methanoprolines and other 3,4-disubstituted prolines

J. J. Vaquero, J. Ezquerra, A. Rubio, 1996 .

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

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

Synthesis of Enantiomerically Pure 4-Substituted Glutamic Acids and Prolines: General Aldol Reaction of Pyroglutamate Lactam Lithium Enolate Mediated by Et2O.cntdot.BF3

C. Pedregal, M. C. Carreño, A. Escribano, 1995 .

Stereoselective hydride reductions of chiral 2-p-tolylsulfinylcycloalkanones

M. C. Carreño, J. G. Ruano, A. Rubio, 1994 .

Reactions of chiral 2-p-tolylsulfinycycloalkanones with AlMe3

J. Fischer, M. C. Carreño, J. G. Ruano, 1991 .

Stereoselective Reductions of 2-Keto Sulfoxides with Hydrides.

C. Pedregal, G. Solladié, M. C. Carreño, 1990 .

Synthesis and reduction of chiral sulfinyl cyclohexanones

M. C. Carreño, J. G. Ruano, A. Rubio, 1987 .

Behaviour of 2-p-tolylsulfinyl cyclohexanols under the pummerer reaction conditions

M. C. Carreño, J. G. Ruano, A. Rubio, 1992 .

New enantioselective approach to the total synthesis of (−)-α-Kainic Acid

J. J. Vaquero, J. Ezquerra, A. Rubio, 1998 .

Design and synthesis of piperidine farnesyltransferase inhibitors with reduced glucuronidation potential.

Mitsunobu Hara, S. Soga, S. Akinaga, 2007, Bioorganic & medicinal chemistry.

Short and efficient enantioselective synthesis of cis and trans pyrrolidine-2,5 dicarboxylic acids

C. Pedregal, J. G. Ruano, J. Ezquerra, 1993 .

Synthesis of chiral cyclic α-p-tolylsulphinyl ketones

C. Pedregal, M. C. Carreño, J. G. Ruano, 1989 .

Asymmetric synthesis of orsellinic acid type macrolides: The example of lasiodiplodin

G. Solladié, M. C. Carreño, J. G. Ruano, 1990 .

Asymmetric synthesis of (S)-zearalenone dimethyl ether, an orsellinic acid type macrolide

C. Pedregal, G. Solladié, M. Maestro, 1991 .

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

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

Synthesis of Chiral Cyclic α‐p‐Tolylsulfinyl Ketones.

C. Pedregal, M. C. Carreño, J. G. Ruano, 1989 .

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

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

(2S,4S)-amino-4-(2,2-diphenylethyl)pentanedioic acid selective group 2 metabotropic glutamate receptor antagonist.

D. Schoepp, C. Pedregal, B. Johnson, 1998, Bioorganic & medicinal chemistry letters.

Abstract 1236: Preclinical characterization of LY3484356, a novel, potent and orally bioavailable selective estrogen receptor degrader (SERD)

Brian E. Mattioni, C. Mur, T. K. Baker, 2021, Experimental and Molecular Therapeutics.

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

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

Imidazo[1,2-b]pyridazines, novel nucleus with potent and broad spectrum activity against human picornaviruses: design, synthesis, and biological evaluation.

C. Hamdouchi, Concha Sánchez-Martínez, M. del Prado, 2003, Journal of medicinal chemistry.