Lin Yan

发表

1-(2,3-Di-O-acetyl-4-chloro-4-deoxy-6-O-tosyl-β-d-galactopyranosyl)propan-2-one methanol 0.25-solvate

Hong-min Liu, Feng-Wu Liu, Lin Yan, 2008, Acta crystallographica. Section E, Structure reports online.

Discovery of N-[(4R)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2,2-dimethyl-3,4-dihydro-2H-pyrano[2,3-b]pyridin-4-yl]-5-methyl-1H-pyrazole-3-carboxamide (MK-5596) as a novel cannabinoid-1 receptor (CB1R) inverse agonist for the treatment of obesity.

L. Shearman, Richard Z. Chen, R. Ball, 2010, Journal of medicinal chemistry.

Highly stereoselective synthesis and structural characterization of new amino sugar derivatives.

Hong-min Liu, Feng-Wu Liu, Lin Yan, 2006, Carbohydrate research.

Synthesis, stereochemical determination and biochemical characterization of the enantiomeric phosphate esters of the novel immunosuppressive agent FTY720.

G. Chrebet, J. Hale, S. Mandala, 2004, Bioorganic & medicinal chemistry.

Dihydro-pyrano[2,3-b]pyridines and tetrahydro-1,8-naphthyridines as CB1 receptor inverse agonists: synthesis, SAR and biological evaluation.

L. Shearman, M. Goulet, T. Fong, 2010, Bioorganic & medicinal chemistry letters.

Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1P receptor subtypes.

G. Chrebet, J. Hale, S. Mills, 2006, Bioorganic & medicinal chemistry letters.

Synthesis of Novel Caged Intramolecular Ketals of β‐C‐Glycopyranosidic Ketones

Hong-min Liu, Feng-Wu Liu, Lin Yan, 2007 .

An efficient synthesis of quinoxaline derivatives from 4-chloro-4-deoxy-alpha-D-galactose and their cytotoxic activities.

Hong-min Liu, G. Dai, Feng-Wu Liu, 2007, Bioorganic & medicinal chemistry letters.

A novel free C-12 higher carbon sugar : asymmetric synthesis and reactivity with nucleophiles

Hong-min Liu, Xiao-ping Song, Fengwu Liu, 2006 .

DNA-binding and cleavage studies of chiral Mn(III) salen complexes

Wenhui Zhou, Lin Yan, Hanwen Liu, 2009 .

Generalizing Glycosylation: Synthesis of the Blood Group Antigens Lea, Leb, and Lex Using a Standard Set of Reaction Conditions

D. Kahne, Lin Yan, 1996 .

Synthesis of furanosyl α-C-glycosides derived from 4-chloro-4-deoxy-α-d-galactose and their cytotoxic activities

Hong-min Liu, G. Dai, Fengwu Liu, 2007 .

p-Methoxybenzyl Ethers as Acid-Labile Protecting Groups in Oligosaccharide Synthesis

D. Kahne, Lin Yan, 1995 .

Design and synthesis of conformationally constrained 3-(N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors.

G. Chrebet, H. Rosen, C. L. Lynch, 2004, Bioorganic & medicinal chemistry letters.

Efficient Synthesis of 2,3‐Disubstituted‐1,3‐benzoxazines by Chlorotrimethylsilane‐Mediated Aza‐Acetalizations of Aromatic Aldehydes

Zhonghua Zhu, Zi-long Tang, Lin Yan, 2013 .

Glycosylation on the Merrifield Resin Using Anomeric Sulfoxides

D. Kahne, Carol M. Taylor, Lin Yan, 1994 .

Prolyl hydroxylase domain-containing protein inhibitors as stabilizers of hypoxia-inducible factor: small molecule-based therapeutics for anemia

J. Hale, Lin Yan, V. J. Colandrea, 2010, Expert opinion on therapeutic patents.

Synthesis and Biological Evaluation of Andrographolide C‐Glycoside Derivatives as α‐Glycosidase Inhibitors

Hong-min Liu, Jin Zhao, Fengwu Liu, 2012 .

SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P1) with enhanced pharmacokinetic properties.

G. Chrebet, J. Hale, S. Mills, 2007, Bioorganic & medicinal chemistry letters.

Carboxylic Acids — Synthesis from Aldehydes, Ketones, and Derivatives (Including Enol Ethers)

Sue-Ing Lin, Ping Liu, Lin Yan, 2008 .

Highly selective and potent agonists of sphingosine-1-phosphate 1 (S1P1) receptor.

G. Chrebet, P. Váchal, J. Hale, 2006, Bioorganic & Medicinal Chemistry Letters.

2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors.

G. Chrebet, C. L. Lynch, J. Hale, 2006, Bioorganic & medicinal chemistry letters.

2‐Aryl(pyrrolidin‐4‐yl)acetic Acids are Potent Agonists of Sphingosine‐1‐phosphate (S1P) Receptors.

Lin Yan, 2006 .

2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists.

J. Hale, S. Mills, S. Mandala, 2006, Bioorganic & medicinal chemistry letters.

Design and synthesis of conformationally constrained 3-(N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors.

G. Chrebet, H. Rosen, C. L. Lynch, 2004, Bioorganic & medicinal chemistry letters.