Hong Lin

发表

B. Snider, Hong Lin, 2012, The Journal of organic chemistry.

Synthesis and structure-activity relationships of imidazo[1,2-a]pyrimidin-5(1H)-ones as a novel series of beta isoform selective phosphatidylinositol 3-kinase inhibitors.

J. F. Mack, J. Luengo, Ramona N Plant, 2012, Bioorganic & medicinal chemistry letters.

Hollow Pt-Ni alloy nanospheres with tunable chamber structure and enhanced activity

Xinggui Zhou, Hexing Li, Hui Li, 2011 .

Nucleoside protein arginine methyltransferase 5 (PRMT5) inhibitors.

J. Luengo, Hong Lin, 2019, Bioorganic & medicinal chemistry letters.

Discovery of Potent and Selective Covalent Protein Arginine Methyltransferase 5 (PRMT5) Inhibitors

J. Luengo, K. Vaddi, Rupa Shetty, 2019, ACS medicinal chemistry letters.

Isoform Selective PI3K-beta Inhibitors

Hong Lin, 2013 .

Rational Design, Synthesis, and SAR of a Novel Thiazolopyrimidinone Series of Selective PI3K-beta Inhibitors.

J. F. Mack, J. Luengo, Ramona N Plant, 2012, ACS medicinal chemistry letters.

Synthesis, characterizations and theoretical analysis of a noncentrosymmetric sulfate

Hong Lin, Yaoguo Shen, Renwen Yan, 2020, Inorganic Chemistry Communications.

[3a,4]-Dihydropyrazolo[1,5a]pyrimidines: Novel, Potent, and Selective Phosphatidylinositol-3-kinase β Inhibitors.

J. Luengo, Ramona N Plant, K. Erhard, 2013, ACS medicinal chemistry letters.

Synthesis and structure-activity relationships of 1,2,4-triazolo[1,5-a]pyrimidin-7(3H)-ones as novel series of potent β isoform selective phosphatidylinositol 3-kinase inhibitors.

J. Luengo, Ramona N Plant, K. Erhard, 2012, Bioorganic & medicinal chemistry letters.

Synthesis of Desmethylamino FR901483

B. Foxman, B. Snider, Hong Lin, 1998 .

Gelsemine: a thought-provoking target for total synthesis.

S. Danishefsky, Hong Lin, 2003, Angewandte Chemie.

Gelsemine: A Thought‐Provoking Target for Total Synthesis

S. Danishefsky, Hong Lin, 2003 .

Synthesis of (±)-7-hydroxylycopodine.

B. Snider, G. Garcia, Hong Lin, 2012, The Journal of organic chemistry.

Explorations in organic chemistry leading to the total synthesis of (+/-)-gelsemine.

S. Danishefsky, Fay W Ng, P. Chiu, 2002, Journal of the American Chemical Society.

The synthesis of (±)-gelsemine

S. Danishefsky, Fay W Ng, Hong Lin, 2002 .

Total Synthesis of (−)-FR901483

B. Snider, Hong Lin, 1999 .

Ordered Mesoporous Ni Nanowires with Enhanced Hydrogenation Activity Prepared by Electroless Plating on Functionalized SBA-15

Hexing Li, S. Xie, W. Dai, 2008 .

Highly concise routes to epothilones: the total synthesis and evaluation of epothilone 490.

T. Chou, S. Danishefsky, W. Tong, 2002, Journal of the American Chemical Society.

Effect of framework aluminum in proton‐ or copper‐exchanged MFI ferrialuminosilicates on their activity for the reduction of nitric oxide with ammonia

T. Yashima, T. Komatsu, Hong Lin, 2000 .

2,3,5-Trisubstituted pyridines as selective AKT inhibitors-Part I: Substitution at 2-position of the core pyridine for ROCK1 selectivity.

J. Luengo, D. Yamashita, D. Heerding, 2010, Bioorganic & medicinal chemistry letters.

Tetrasubstituted pyridines as potent and selective AKT inhibitors: Reduced CYP450 and hERG inhibition of aminopyridines.

Sharad Verma, Kristin K. Brown, Anthony E Choudhry, 2010, Bioorganic & medicinal chemistry letters.

Exploiting Binding-Site Arginines in Drug Design: Recent Examples.

J. Luengo, Hong Lin, 2020, Bioorganic & medicinal chemistry letters.

Discovery of a Novel 2,6-Disubstituted Glucosamine Series of Potent and Selective Hexokinase 2 Inhibitors.

Yong Jiang, Jacques Briand, Junya Qu, 2016, ACS medicinal chemistry letters.

2,3,5-Trisubstituted pyridines as selective AKT inhibitors. Part II: Improved drug-like properties and kinase selectivity from azaindazoles.

Kristin K. Brown, J. Luengo, Rakesh Kumar, 2010, Bioorganic & medicinal chemistry letters.