X. Qian

发表

Synthesis of ethyl 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylate via regioselective dipolar cycloaddition

Antonio Ramirez, O. Soltani, Michael A. Schmidt, 2012 .

Adventures in Atropisomerism: Total Synthesis of a Complex Active Pharmaceutical Ingredient with Two Chirality Axes.

Jason M. Stevens, Thomas M. Razler, Antonio Ramirez, 2018, Organic letters.

A mild synthesis of [1,2,4]triazolo[4,3-a]pyridines

Michael A. Schmidt, X. Qian, 2013 .

Stereoselective total synthesis of topographically constrained designer amino acids: 2′, 6′-dimethyl-β-methyltyrosines

V. Hruby, L. Boteju, K. Russell, 1995 .

Asymmetric synthesis of unusual amino acids: Synthesis of optically pure isomers of N-indole- (2-mesitylenesulfonyl)-β-methyltryptophan

V. Hruby, L. Boteju, X. Qian, 1994 .

Probing the Stereochemical Requirements for Receptor Recognition of δ Opioid Agonists through Topographic Modifications in Position 1

R. Horváth, V. Hruby, H. Yamamura, 1996 .

A stereoselective synthesis of BMS-262084, an azetidinone-based tryptase inhibitor.

M. Saindane, B. Zheng, Brian Burke, 2002, The Journal of organic chemistry.

A stereoselective synthesis of (S)-2-(((3-fluoro-4-methylphenoxy)carbonyl)(1-(4-((5-methyl-2-phenyloxazol-4-yl)methoxy)phenyl)ethyl)amino)acetic acid, a highly potent PPAR α/γ dual agonist

J. Shabaker, Junying Fan, Keming Zhu, 2015 .

C2-symmetrical tetrahydroxyazepanes as inhibitors of glycosidases and HIV/FIV proteases.

M. Fitzgerald, F. Morís-Varas, C. Wong, 1996, Bioorganic & medicinal chemistry.

SYNTHESIS OF C2-SYMMETRICAL POLYHYDROXYAZEPANES AS INHIBITORS OF GLYCOSIDASES

Chi‐Huey Wong, F. Morís-Varas, X. Qian, 1996 .

Enzymatic/Chemical Synthesis and Biological Evaluation of Seven-Membered Iminocyclitols

Chi‐Huey Wong, F. Morís-Varas, X. Qian, 1996 .

Development of a Two-Step, Enantioselective Synthesis of an Amino Alcohol Drug Candidate

Chenchi Wang, C. Hang, Zhiwei Guo, 2015 .

Enzyme-Catalyzed Hydrolysis of Bicycloheptane and Cyclobutene Diesters to Monoesters

Zhiwei Guo, A. Goswami, Michael K Wong, 2014 .

Novel scaffolds for non-peptide mimetics of δ opioid receptor agonists based on peptide leads

V. Hruby, H. Yamamura, D. Stropova, 1996, Regulatory Peptides.

A three-dimensional model of the delta-opioid pharmacophore: comparative molecular modeling of peptide and nonpeptide ligands.

V. Hruby, X. Qian, M. Shenderovich, 2000, Biopolymers.

Antinociceptive Activity of [β-Methyl-2′,6′-dimethyltyrosine1]-Substituted Cyclic [d-Pen2,d-Pen5]Enkephalin and [d-Ala2,Asp4]Deltorphin Analogs

V. Hruby, F. Porreca, E. Bilsky, 2000 .

Antinociceptive Activity of [ b-Methyl-2 9 , 6 9-dimethyltyrosine 1 ]-Substituted Cyclic [ D-Pen 2 , D-Pen 5 ] Enkephalin and [ DAla 2 , Asp 4 ] Deltorphin Analogs 1

V. Hruby, F. Porreca, E. Bilsky, 2000 .

Approaches to the asymmetric synthesis of unusual amino acids.

V. Hruby, X. Qian, 1994, Methods in molecular biology.

Approaches to the Asymmetric Synthesis of Unusual Amino Acids

V. Hruby, X. Qian, 1995 .

Topographical design of message domain pharmacophores of δ opioid agonists provide insights into the stereochemical requirements for recognizing δ opioid receptor subtypes

R. Horváth, V. Hruby, B. Lou, 1995 .

Surface modification of montmorillonite and application to the preparation of polybutadiene/montmorillonite nanocomposites

Weiqing Zhang, Mingyi Liao, X. Qian, 2007 .

Antinociceptive activity of [beta-methyl-2', 6'-dimethyltyrosine(1)]-substituted cyclic [D-Pen(2), D-Pen(5)]Enkephalin and [D-Ala(2),Asp(4)]Deltorphin analogs.

V. Hruby, F. Porreca, E. Bilsky, 2000, Journal of Pharmacology and Experimental Therapeutics.

Chemical and Enzymatic Resolution of (R,S)-N-(tert-Butoxycarbonyl)-3-hydroxymethylpiperidine

Ramesh N. Patel, A. Goswami, K. D. Mirfakhrae, 2001 .

Topographical considerations in de novo design of peptides

V. Hruby, F. Porreca, E. Bilsky, 2002 .

Newly discovered stereochemical requirements in the side-chain conformation of delta opioid agonists for recognizing opioid delta receptors.

R. Horváth, B. Lou, A. Misicka, 1994, Journal of medicinal chemistry.