Mihai Dumitru Azimioara

发表

Bioorganic & Medicinal Chemistry Letters

Phil B. Alper, Mihai Dumitru Azimioara, Christopher Cow, 2001, Bioorganic & Medicinal Chemistry Letters.

1,3,5-Trisubstituted aryls as highly selective PPARδ agonists

R. Epple, B. Bursulaya, R. Russo, 2006 .

X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reduction

E. Corey, S. Sarshar, Mihai Dumitru Azimioara, 1992 .

Novel tricyclic pyrazolopyrimidines as potent and selective GPR119 agonists.

P. McNamara, S. Joseph, R. Epple, 2014, Bioorganic & medicinal chemistry letters.

An efficient synthesis of a 4'-phosphonodifluoromethyl-3'-formyl-phenylalanine containing SRC SH2 ligand.

D. Holt, R. Bohacek, M. Botfield, 1999, Bioorganic & medicinal chemistry letters.

Novel bisaryl substituted thiazoles and oxazoles as highly potent and selective peroxisome proliferator-activated receptor delta agonists.

J. Wityak, E. Saez, R. Epple, 2010, Journal of medicinal chemistry.

A small molecule–kinase interaction map for clinical kinase inhibitors

L. Wodicka, D. Lockhart, P. Zarrinkar, 2005, Nature Biotechnology.

A HYPOTHESIS FOR CONFORMATIONAL RESTRICTION IN COMPLEXES OF FORMYL COMPOUNDS WITH BORON LEWIS ACIDS. EXPERIMENTAL EVIDENCE FOR FORMYL CH--O AND CH--F HYDROGEN BONDS

E. Corey, J. Rohde, Mihai Dumitru Azimioara, 1997 .

Discovery of Orally Active Hydroxyethylamine Based SPPL2a Inhibitors.

Daniel R. Beisner, R. Epple, B. Wen, 2019, ACS medicinal chemistry letters.

The structure of the 2-methylacrolein boron trifluoride complex in the crystalline phase and in solution

E. Corey, S. Sarshar, T. Loh, 1992 .

The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studies

E. Corey, T. Loh, M. C. Noe, 1992 .

A Novel Synthesis of the Fluorene Skeleton

E. Corey, Mihai Dumitru Azimioara, A. Fischer, 1997 .

X-ray Crystal and NMR Structure of a Highly Reactive Bidentate 1,2-Diamine−OsO4 Complex, Formally a 20-Electron Outer Valence Shell Species. Mechanistic Implications for the 1,2-Diamine-Accelerated Dihydroxylation of Olefins by OsO4

E. Corey, S. Sarshar, M. C. Noe, 1996 .

Composés et compositions pouvant servir de modulateurs de l'activité du gpr119

Mihai Dumitru Azimioara, Phillip B. Alper, Christopher Cow, 2010 .

A novel mechanism-based mammalian cell assay for the identification of SH2-domain-specific protein-protein inhibitors.

R. Rickles, S. Violette, M. Zoller, 1998, Chemistry & biology.

Structure-based design of novel bicyclic nonpeptide inhibitors for the src SH2 domain.

M. Hatada, S. Violette, R. Bohacek, 2000, Journal of medicinal chemistry.

Composés et compositions tels que des modulateurs d'une activité gpr119

Mihai Dumitru Azimioara, Songchun Jiang, Phillip B. Alper, 2008 .

Structure-based design of an osteoclast-selective, nonpeptide src homology 2 inhibitor with in vivo antiresorptive activity.

M. Hatada, S. Violette, R. Bohacek, 2000, Proceedings of the National Academy of Sciences of the United States of America.

3,4,5-Trisubstituted isoxazoles as novel PPARdelta agonists. Part 2.

J. Wityak, A. Kreusch, E. Saez, 2006, Bioorganic & medicinal chemistry letters.

1,3,5-Trisubstituted Aryls as Highly Selective PPARδ Agonists.

R. Epple, B. Bursulaya, R. Russo, 2006 .